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In one aspect the present invention relates to the use of viral promoters in the expression of chimeric genes in plant cells. In another aspect this invention relates to chimeric genes which are capable of being expressed in plant cells, which utilize promoter regions derived from viruses which are capable of infecting plant cells. One such virus comprises the cauliflower mosaic virus CaMV. Two different promoter regions have been derived from the CaMV genome and ligated to heterologous coding sequences to form chimeric genes. These chimeric genes have been shown to be expressed in plant cells. This invention also relates to plant cells, plant tissue, and differentiated plants which contain and express the chimeric genes of this invention. This invention is in the fields of genetic engineering and plant biology. A virus is a microorganism comprising single or double stranded nucleic acid DNA or RMA contained within a protein and possibly lipid shell called a 'capsid' or 'coat'. A virus is smaller than a cell, and it does not contain most of the components and substances necessary to conduct most biochemical processes. Instead, a virus infects a cell and uses the cellular processes to reproduce itself. The following is a simplified description of how a DNA-containing virus infects a cell; RNA viruses will be disregarded in this introduction for the sake of clarity. First, a virus attaches to or enters a cell, normally called a 'host' cell. The DNA from the virus and possibly the entire viral particle enters the host cell where it usually operates as a plasmid a loop of extra-chromosomal DNA. Some of these polypeptides are assembled into new capsids, while others act as enzymes to catalyze various biochemical reactions. The viral DNA is also replicated and assembled with the capsid polypeptides to form new viral particles. These viral particles may be released gradually by the host cell, or they may cause the host cell to lyse and release them. The released viral particles subsequently infect new host cells. For more background information on viruses see, e. As used herein, the term 'virus' includes phages and viroids, as well as replicative intermediates. For example, a DNA strand created by using a viral RNA strand as a template, or by chemical synthesis to create a known sequence of bases determined by analyzing viral DNA, would be regarded as viral nucleic acid. The host range of any virus i. Some viruses are capable of efficient infection of only certain types of bacteria; other viruses can infect only plants, and may be limited to certain genera; some viruses can infect only mammalian cells. Viral infection of a cell requires more than mere entry of the viral DNA or RNA into the host cell; viral particles must be reproduced within the cell. Through various assays, those skilled in the art can readily determine whether any particular type of virus is capable of infecting any particular genus, species, or strain of cells. As used herein, the term 'plant virus' is used to designate a virus which is capable of infecting one or more types of plant cells, regardless of whether it can infect other types of cells. With the possible exception of viroids which are poorly understood at present , every viral particle must contain at least one gene which can be 'expressed' in infected host cells. Most viruses have about 5 to 10 different genes, all of which are expressed in a suitable host cell. In order to be expressed in a cell, a gene must have a promoter which is recognized by certain enzymes in the cell. Gene promoters are discussed in some detail in the parent application Ser. Those skilled in the art recognize that the expression of a particular gene to yield a polypeptide is dependent upon two distinct cellular processes. A region of the 5' end of the gene called the promoter, initiates transcription of the gene to produce a mRNA transcript. The mRNA is then translated at the ribosomes of the cell to yield an encoded polypeptide. Therefore, it is evident that although the promoter may function properly, ultimate expression of the polypeptide depends at least in part on post-transcriptional processing of the mRNA transcript. Promoters from viral genes have been utilized in a variety of genetic engineering applications. For example, chimeric genes have been constructed using various structural sequences also called coding sequences taken from bacterial genes, coupled to promoters taken from viruses which can infect mammalian cell the most commonly used mammalian viruses are designated as Simian Virus 40 SV40 and Herpes Simplex Virus HSV. These chimeric genes have been used to transform mammalian cells. See, e. In addition, chimeric genes using promoters taken from viruses which can infect bacterial cells have been used to transform bacterial cells; see, e. Several researchers have theorized that it might be possible to utilize plant viruses as vectors for transforming plant cells. In general, a 'vector' is a DNA molecule useful for transferring one or more genes into a cell. Usually, a desired gene is inserted into a vector, and the vector is then used to infect the host cell. Several researchers have theorized that it might be possible to create chimeric genes which are capable of being expressed in plant cells, by using promoters derived from plant virus genes. However, despite the efforts of numerous research teams, prior to this invention no one had succeeded in 1 creating a chimeric gene comprising a plant virus promoter coupled to a heterologous structural sequence and 2 demonstrating the expression of such a gene in any type of plant cell. Gardner et al, ; Hohn et al, In its most common form, the CaMV genome is about bp long. However, various naturally occurring infective mutants which have deleted about bp have been discovered; see Howarth et al The entire CaMV genome is transcribed into a single mRNA, termed the 'full-length transcript' having a sedimentation coefficient of about 35S. The promoter for the full-length mRNA hereinafter referred to as 'CaMV 35S ' is located in the large intergenic region about 1 kb counterclockwise from Gap 1 see Guilley et al, In one aspect, the present invention relates to the use of viral promoters in the expression of chimeric genes in plant cells. These chimeric genes have been proven to be expressed in plant cells. This invention also relates to plant cells, plant tissue including seeds and propagules , and differentiated plants which have been transformed to contain viral promoters and express the chimeric genes of this invention, and to polypeptides that are generated in plant cells by the chimeric genes of this invention. The figures herein are schematic representations; they have not been drawn to scale. In one preferred embodiment of this invention, a chimeric gene was created which contained the following elements:. Plasmid pMON was inserted into an Agrobacterium tumefaciens cell, where it formed a co-integrate Ti plasmid by means of a single crossover event with a Ti plasmid in the A. Some of the plant cells were genetically transformed, causing them to become resistant to an antibiotic kanamycin at concentrations which are toxic to untransformed plant cells. A similar chimeric gene was created and assembled in a plasmid designated as pMON This chimeric gene resembled the gene in pMON, with two exceptions:. The construction of this chimeric gene is described in Example 2. This gene was inserted into A. Its level of expression was apparently higher than the expression of the similar gene in pMON, as assayed by growth on higher concentrations of kanamycin. In an alternate preferred embodiment of this invention, a chimeric gene was created comprising. The assembly of this chimeric gene is described in Example 3. This gene was inserted into plant cells and it caused them to become resistant to kanamycin. Petunia plants cannot normally be infected by CaMV. Those skilled in the art may determine through routine experimentation whether any particular plant viral promoter such as the CaMV promoter will function at satisfactory levels in any particular type of plant cell, including plant cells that are outside of the normal host range of the virus from which the promoter was derived. It is possible to regenerate genetically transformed plant cells into differentiated plants. One method for such regeneration was described in U. That application was filed simultaneously with, and incorporated by reference into, the parent application of this invention. The methods of application Ser. It is possible to extract polypeptides generated in plant cells by chimeric genes of this invention from the plant cells, and to purify such extracted polypeptides to a useful degree of purity, using methods and substances known to those skilled in the art. Those skilled in the art will recognize, or may ascertain using no more than routine experimentation, numerous equivalents to the specific embodiments described herein. Such equivalents are within the scope of this invention, and are covered by the claims below. Shepherd, University of California, Davis. To the best of Applicants' knowledge and belief, these plasmids designated as pOS1 were obtained by inserting the entire genome of a CaMV strain designated as CM Howarth et al, into the Sal I restriction site of a pBR plasmid Bolivar et al, Three small fragments were purified after electrophoresis on an 0. The smallest fragment, about bp in size, contains the 19S promoter. After various manipulations which did not change the sequence of this fragment shown in FIG. Plasmid pMON was inserted into E. The foregoing methods are described in detail in a separate application, entitled 'Plasmids for Transforming Plant Cells' Ser. The co-cultivated petunia cells were cultured on media containing kanamycin, an antibiotic which is toxic to petunia cells. These results were confirmed by Southern blot analysis of transformed plant cell DNA. Plasmid pMON72 was obtained by inserting a 1. This fragment was digested with MboI to obtain a bp fragment. After transformation of E. A colony containing a plasmid with the desired structure was identified. The resulting overhanging end was filled in to create a blunt end by treatment with Klenow polymerase and the four deoxy-nucleotide triphosphates dNTP's , A, T, C, and G. The Klenow polymerase was inactivated by heat, the fragment was digested with PstI, and a 3. This fragment was ligated with the 3. The mixture was used to transform E. Plasmid pMON was inserted into A. The pMON plasmid formed a cointegrate plasmid with the Ti plasmid by means of a single crossover event. Cells which contain this co-integrate plasmid have been deposited with the American Type Culture Center, and have been assigned ATCC accession number A fragment which contains the chimeric gene of this invention can be obtained by digesting the co-integrate plasmid with HindIII and EcoRI, and purifying the 1. This fragment contained the 35S promoter region and part of the 5' non-translated region. This polyadenylation region was removed as follows: pMON50 was digested with AvaII and an bp fragment was purified. The 3. This fragment does not carry the polyadenylation region for the 35S RNA. One recombinant phage, M12, carried the bp fragment in the orientation shown on FIG. These plasmids differ only in the direction of the chimeric gene orientation. These plasmids were used to transform petunia cells, as described in Example 1. Chimeric genes carrying the nopaline synthase NOS promoter or the cauliflower mosaic virus full-length transcript promoter CaMV 35S were constructed. In both cases, the promoters, which contain their respective 5' non-translated regions were joined to a NPTII coding sequence in which the bacterial 5' leader had been modified so that a spurious ATG translational initiation signal Southern and Berg, has been removed. The CM strain is a naturally occurring deletion mutant of strain CM The nucleotide sequence of the CM Gardner et al. The nucleotide sequences of the 35S promoter regions of these three isolates are essentially identical. In the following the nucleotide numbers reflects the sequence of Gardner et al. Site directed mutagenesis Zoller and Smith, was then used to introduce a G at nucleotide to create a BglII site. The 35S promoter fragment was then excised from the M13 as a bp EcoRI-BglII fragment which contains the 35S promoter, 30 nucleotides of the 5' non-translated leader but does not contain any of the CaMV translational initiators nor the 35S transcript polyadenylation signal that is located nucleotides downstream from the start of transcription Covey et al. The CaMV 35S promoter sequence described above is listed below. The 35S promoter fragment was joined to a 1. These plasmids were transferred in E. Cocultivation of Petunia protoplasts with A. Following low speed centrifugation, cesium chloride was added to the supernatant 0. The ethidium bromide was extracted with isopropanol, the DNA was dialyzed, and ethanol precipitated. The fragments were separated by electrophoresis on a 0. Plant leaves were frozen in liquid nitrogen and ground to a fine powder with a mortar and pestle. The crude homogenate was mixed for 10 min and the phases separated by centrifugation. The aqueous phase then was re-extracted with an equal volume of PCI. The aqueous phase was ethanol precipitated with one tenth volume of 3M NaAcetate and 2. The nucleic acid pellet was resuspended in water. An equal volume of 4M lithium chloride LiCl was added and the mix was placed on ice for 1 hour or overnight. Following centrifugation, the pellet was resuspended in water the LiCl precipitation repeated 3 times. The final LiCl pellet was resuspended in water and ethanol precipitated. The RNAs were electrophoresed in 1. The nick-translated DNAs used as probes were the 1. The gel overlay assay was used to determine the steady state level of NPTII enzyme activity in each plant. Several parameters were investigated for optimizing the sensitivity of the assay in plant tissue. Early observations showed that the level of NPTII activity varied between leaves from different positions on the same plant. This variability was minimized when the plant extract was made from pooled tissue. A paper hole punch was used to collect 15 disks from both young and old leaves. Grinding the plant tissue in the presence of micro-beads Ferro Corp rather than glass beads increased the plant protein yield 4-fold. Supplementing plant cell extracts with ug per lane of bovine serum albumin BSA , resulted in a linear response; NPTII activity increased proportionately as plant protein levels increased. The addition of BSA appears to stabilize the enzyme, resulting in a fold increase in the sensitivity of the assay. Elimination of SDS from the extraction buffer resulted in a 2-fold increase in assay sensitivity. Leaf disks were pooled from each plant for the assay. Following centrifugation in a microfuge for 20 minutes, total protein was determined using the Bradford assay. The polyacrylamide gel was equilibrated for 30 minutes in water and then 30 minutes in reaction buffer 67 mM TRIS-maleate pH 7. After 1 hour at room temperature a sheet of Whatman P81 paper, two sheets of Whatman 3MM paper, a stack of paper towels and a weight were put on top of the agarose gel. The phosphorylated neomycin is positively charged and binds to the P81 phosphocellulose ion exchange paper. The paper was air dried and exposed to XAR-5 film. The NPTII transcript levels and enzyme activities in two sets of transgenic petunia plants were compared. In several of the transgenic plants, there is a substantial variation in both RNA and enzyme levels which cannot be accounted for by the slight difference in gene copy number. Such 'position effects' have been reported in transgenic mice and fruit flies and have not yet been adequately explained at the molecular level. Although, there is not a clear correlation between insert copy number and level of chimeric gene expression, the fact that 4 of the 7 pMON transgenic plants contain 2 copies of the NOS-NPTII-NOS gene would suggest that the differential expression of the CaMV 35S promoter is actually slightly underestimated in these studies. The constructs described in this comparative example have identical coding regions and 3' non-translated regions, indicating that the differences in the steady state transcript levels of these chimeric genes is a result of the 5' sequences. As in the above example, the promoters contained their respective 5' non-translated regions and were joined to a NPTII coding sequence in which the bacterial 5' leader had been modified to remove a spurious ATG translational initiation signal. The references to nucleotide numbers in the following discussion are those for the sequence of CM Gardner et al. The resulting 1. The resulting plasmid is pMON The only difference is the sequence of the 5' nontranslated leader sequence which in pMON contains the extra ATG signal found in the bacterial leader of NPTII and contains extra bases from the synthetic linker and bacterial leader sequence. Petunia leaf discs were transformed and plants regenerated as described above. Quantitation was done by scintillation counting of 32 P-neomycin, the end product of neomycin phosphotransferase activity. Covey, G. Lomonosoff and R. Hull Nucleic Acids Res. Fraley, et al. USA Fraley, R. Horsch, A. Matzke, M. Chilton, W. Chilton and P. Sanders Plant Molecular Biology 3, Guilley, G. Joward, K. Richards and L. Hirth Cell 21, Gardner et al, Nucleic Acids Research Vol. Springer Verlag, N. Matthews ed. Plant Virology Academic Press, N. Stryer, Biochemistry, 2nd. Freeman and Co. San Francisco, We claim: 1. A chimeric gene which is expressed in plant cells comprising a promoter from a cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter isolated from CaMV protein-encoding DNA sequences and a CaMV 19S promoter isolated from CaMV protein-encoding DNA sequences, and a structural sequence which is heterologous with respect to the promoter. A chimeric gene of claim 1 in which the promoter is the CaMV 35S promoter. A chimeric gene of claim 1 in which the promoter is the CaMV 19S promoter. A plant cell which comprises a chimeric gene that contains a promoter from cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter and a CaMV 19S promoter, wherein said promoter is isolated from CaMV protein-encoding DNA sequences, and a structural sequence which is heterologous with respect to the promoter. A plant cell of claim 4 in which the promoter is the CaMV 35S promoter. A plant cell of claim 4 in which the promoter is the CaMV 19S promoter. An intermediate plant transformation plasmid which comprises a region of homology to an Agrobacterium tumefaciens vector, a T-DNA border region from Agrobacterium tumefaciens and a chimeric gene, wherein the chimeric gene is located between the T-DNA border and the region of homology, said chimeric gene comprising a promoter from cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter and a CaMV 19S promoter, and a structural sequence which is heterologous with respect to the promoter. A plant transformation vector which comprises a disarmed plant tumor inducing plasmid of Agrobacterium tumefaciens and a chimeric gene, wherein the chimeric gene contains a promoter from cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter and a CaMV 19S promoter, and a structural sequence which is heterologous with respect to the promoter. A plant transformation vector of claim 8 in which the promoter is the CaMV 35S promoter. A plant transformation vector of claim 8 in which the promoter is the CaMV 19S promoter. The chimeric gene of claim 1 comprising in the 5' to 3' direction: 1 the CaMV 35S promoter,. The chimeric gene of claim 1 comprising in the 5' to 3' direction: 1 the CaMV 19S promoter,. B a DNA sequence of interest heterologous to A , wherein B is under the regulatory control of A when said construct is transcribed in a plant cell. A chimeric gene which is transcribed and translated in plant cells, said chimeric gene comprising a promoter from cauliflower mosaic virus, said promoter selected from the group consisting of: a a CaMV 35S promoter region free of CaMV protein-encoding DNA sequences and. A chimeric gene which is transcribed in plants cells comprising a promoter from a cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter free of CaMV protein-encoding DNA sequences and a CaMV 19S promoter free of CaMV protein-encoding DNA sequences, a DNA sequence which is heterologous with respect to the promoter and a 3' non-translated polyadenylation signal sequence. A plant cell which comprises a chimeric gene where said chimeric gene comprises a promoter from cauliflower mosaic virus, said promoter selected from the group consisting of a CaMV 35S promoter and a CaMV 19S promoter, wherein said promoter is free of CaMV protein-encoding DNA sequences, and a DNA sequence which is heterologous with respect to the promoter and a 3' non-translated polyadenylation signal sequence. An intermediate plasmid of claim 7 in which the promoter is the CaMV 19S promoter. An intermediate plasmid of claim 7 in which the promoter is the CaMV 35S promoter. USA Continuation. USA en. Methods and compositions for the production of stably transformed, fertile monocot plants and cells thereof. Plant promoter useful for directing the expression of foreign proteins to the plant epidermis. WOA1 en. DNA sequences from potato encoding solanidine UDP-glucose glucosyltransferase and use to reduce glycoalkaloids in solanaceous plants. Method for producing immunoglobulins containing protection proteins in plants and their use. Anthranilate synthase gene and method of use thereof for conferring tryptophan overproduction. USB1 en. WOA2 en. Recombinant, biologically active human zone pellucida proteins 3 hzp3 to test male fertility. Human zona pellucida proteins and methods of their use in diagnoising male infertility. Moss genes from physcomitrella patens encoding proteins involved in the synthesis of tocopherols and carotenoids. USB2 en. Production of genetically-controlled herbicide resistance in cotton plants in the absence if genetic engineering. Nucleic acid sequences encoding proteins associated with abiotic stress response. Methods and compositions for detection of specific genetic constructs in plant transformation events. Transgenic plants containing molecular decoys that alter protein content therein. Nucleic acid sequences encoding proteins associated with abiotic stress response and plant cells and plants with increased tolerance to environmental stress. Novel nucleic acid sequences and their use in methods for achieving pathogen resistance in plants. Novel immunoadhesins for treating and prventing toxicity and pathogen-mediated diseases. Method of reducing the harmful effects of orally or transdermally delivered nicotine. Method for producing polyunsaturated c20 and c22 fatty acids with at least four double bonds in transgenic plants. Method for the stable expression of nucleic acids in transgenic plants, controlled by a parsley-ubiquitin promoter. EPA2 en. Use of armadillo repeat arm1 polynucleotides for obtaining pathogen resistance in plants. Chimeric toxin receptor proteins and chimeric toxin receptor proteins for treatment and prevention of anthrax. Nucleic acid molecules encoding a branching enzyme comprising bacteria of the genus Neisseria and method for producing alpha Manipulation of the nitrogen metabolism using ammonium transporter or glucose 6-phosphate deshydrogenases or farnesyl phosphate synthetase fpp. Method for increasing resistance of monocot plants against abiotic stresses, tps plant gene constructs, and transformants. Msca1 nucleotide sequences impacting plant male fertility and method of using same. Reversion of the negative selective effect of negative marker proteins as selection procedure. Nucleic acid sequences encoding proteins associated with abiotic stress response and plant cells and plants with increased tolerance to environmantal stress. EPA1 en. Nucleic acid sequences encoding proteins associated with abiotic stress response and plant cells and plants with in-creased tolerance to environmental stress. Isolation and characterization of a novel pythium omega 3 desaturase with specificity to all omega 6 fatty acids longer than 18 carbon chains. Method for producing polyunsaturated fatty acids in transgenic non-human organisms. DET5 en. Use of subtilisin RNR9 polynucleotides for achieving a pathogen resistance in plants. Metallothionein gene conferring abiotic stress tolerance in plants and uses thereof. Regulatory nucleic acid molecules for enhancing seed-specific gene expression in plants promoting enhanced polyunsaturated fatty acid synthesis. Novel immunoadhesins for treating and preventing toxicity and pathogen-mediated diseases. Lipid metabolism proteins, combinations of lipid metabolism proteins and applications thereof. Polypeptides involved in regulation of sugar and lipid metabolism and methods of use VIII. Plants with increased yield and increased tolerance to environmental stress IY-B. A gene from Solanum bulbocastanum conferring resistance to Phytophthora infestans. Arabidopsis genes encoding proteins involved in sugar and lipid metabolism and methods of use. Alteration of tobacco alkaloid content through modification of specific cytochrome p genes. New vegetable acyltransferases specifically for long-chain polyunsaturated fatty acids. Process for the production of delta5-unsaturated fatty acids in transgenic organisms. Use of stomatin STM1 polynucleotides for achieving a pathogen resistance in plants. Methods and means to modify a plant genome at a nucleotide sequence commonly used in plant genome engineering. Increased yield plants by increasing or generating one or more activities in a plant or part thereof. Method for producing a transgenic cell with increased content of gamma-aminobutyric acid GABA. Desaturases and methods of producing polyunsaturated fatty acids in transgenic organisms. Fad2 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks. Chimeric promoters comprising MYB10 repeat element and methods for regulating plant gene expression. Compositions and methods of use of acc oxidase polynucleotides and polypeptides. Methods and compositions for the improvement of plant tolerance to environmental stresses. Alteration of tobacco alkaloid content through modification of specific cytochrome P genes. Method to produce acetyldiacylglycerols ac-TAGs by expression of an acetyltransferase gene isolated from Euonymus alatus burning bush. Transgenic plants with engineered redox sensitive modulation of photosynthetic antenna complex pigments and methods for making the same. Plants comprising wheat g-type cytoplasmic male sterility restorer genes, molecular markers and uses thereof. Nucleic acid molecules that target the vacuolar atpase c subunit and confer resistance to coleopteran pests. Pre-mrna processing factor 8 prp8 nucleic acid molecules to control insect pests. Nucleic acid molecules that target the rho1 small gtp-binding protein and confer resistance to coleopteran pests. Nucleic acid molecules that target the vacuolar atphase h subunit and confer resistance to coleopteran pests. Fad3 performance loci and corresponding target site specific binding proteins capable of inducing targeted breaks. Gene underlying the number of spikelets per spike qtl in wheat on chromosome 7a. Plants comprising wheat g-type cytoplasmic male sterility restorer genes and uses thereof. Methods and compositions for short stature plants through manipulation of gibberellin metabolism to increase harvestable yield. DEU1 en. Compositions and methods for altering flowering and plant architecture to improve yield potential. Proteins for regulation of symbiotic infection and associated regulatory elements. Regulatory nucleic acid molecules for modifying gene expression in cereal plants. Increasing gene editing and site-directed integration events utilizing meiotic and germline promoters. Production of medium chain length polyhydroxyalkanoates from fatty acid biosynthetic pathways. Plant artificial chromosome, its use and method for producing plant artificial chromosome. EPA3 en. Methods for enhancing segregation of transgenes in plants and compositions thereof. Hydroxypyruvate reductase promoter elements and methods of use thereof in plants. PTT en. DED1 en. EPB1 en. ARA1 en. USA1 en. Transgenic plants expressing cytokinin biosynthetic genes and methods of use therefor. Eukaryotic translation initiation factor gene regulatory elements for use in plants. Adenylate translocator protein gene non-coding regulatory elements for use in plants. CAA1 en. Recombinant dna for expression of proteins for imparting enhanced agronomic traits to transgenic plants. AUB2 en. EPA4 en. MXA en. Extracted whole corn kernels and improved processed and processable corn produced thereby. Generation of high polyhydroxybutrate producing oilseeds with improved germination and seedling establishment. BRB1 en. Rnai for the control of phytopathogenic fungi and oomycetes by inhibiting the expression of cyp51 genes. HUET2 en. Transgenic land plants comprising a putative bicarbonate transporter protein of an edible eukaryotic algae. Transgenic land plants comprising enhanced levels of mitochondrial transporter protein. JPA en. ILA en. Compositions and methods for controlling t-dna copy number in transformed plants. Selective genetic markers for eucaryotic cells,method for implementing such markers and application of cells containing such marker to the production of proteins determined after their transformation by a corresponding dna. Process for the introduction of expressible genes into plant cell genomes and agrobacterium strains carrying hybrid ti plasmid vectors useful for this process. Barton et al. Plant Physiol. Beck et al. Berry Lowe et al. Berry-Lowe et al. Bevan et al. Cairns et al. Chilton et al. Colbere Garapin et al. Colbere Gerapin et al, J. Colbere-Garapin et al. Colbere-Gerapin et al, J. Condit et al. Davey et al. De Greve et al. DeGreve et al. Depicker et al. Dix et al. Fraley et al. Franck et al. Gardner, R. Garfinkel et al. Goodman et al. Science 48 Groneborn et al. Guilley et al. Cell 30 3 : Hernalsteens et al. Herrera Estrela et al. Herrera Estrella et al. Herrera-Estrella et al. Hohn et al. Holsters et al. Howell et al. Jimenez et al. Kemp et al. Larkins et al. Lebeurier et al. Leemans et al. Leemans, Universite Libre de Bruxelles, Thesis, 1 25; Leemans, Universite Libre de Bruxelles, Thesis, ; Liu et al. Maliga et al. Matzke et al. McKnight et al. Meagher et al. Mulligan et al. O Hare et al. Old et al. Press, 1st ed. Press, 2nd Ed. Olszewski et al. Otten et al. Portetelle et al. Schell et al. Schroeder at al. Ursic et al. Watson, ' Molecular Biology of the Gene ' 3rd ed. Benjamin, Inc. Watson, Molecular Biology of the Gene 3rd ed. Willmitzer et al. Wilmitzer et al. Zambryski et al. EMBO J 2 12 : Method of preparing fertile transgenic corn plants by microprojectile bombardment. USHH1 en. Methods of producing human or animal food from stably transformed, fertile maize plants. Methods and compositions for the production of stably transformed fertile monocot plants and cells thereof. USREE1 en. Method for producing immunoglobulins containing protection proteins and their use. Regulation of quinolate phosphoribosyl transferase expression by transformation with a tobacco quinolate phosphoribosyl transferase nucleic acid. Methods and compositions for protein production in tobacco plants with reduced nicotine. Method for producing stably transformed duckweed using microprojectile bombardment. Recombinant, biologically active human zona pellucida protein 3 HZP3 to test male fertility. Genetically-controlled herbicide resistance in cotton plants in the absence of genetic engineering. BctHgg cotton displaying genetically-controlled naturally-occurring herbicide resistance, method for transfer, and method of use. Human zona pellucida proteins and methods of their use in diagnosing male infertility. Nucleic acid sequences and their use in methods for achieving pathogen resistance in plants. Method for increasing resistance of monocot plants against abiotic stresses, TPSP fusion enzyme gene constructs, and transformants. Nucleic acid for plant expression of a fusion protein comprising hydroxyproline O-glycosylation glycomodule. Process for decreasing verbascose in a plant by expression of a chloroplast-targeted fimD protein. Nucleic acid molecules encoding polypeptides involved in regulation of sugar and lipid metabolism and methods of use VIII. Plants transformed with a nucleic acid encoding chloroplastic fructose-1,6-bisphosphatase having increased yield, and a method for making the same. Plants transformed with SYT-polypeptide having increased yield under abiotic stress and a method for making the same. Pythium omega 3 desaturase with specificity to all omega 6 fatty acids longer than 18 carbon chains. Desaturases and process for the production of polyunsaturated fatty acids in transgenic organisms. New fatty acid desaturases, elongases, elongation components and applications thereof.
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