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  • GreenlabprotocolforvacuuminfiltrationtransformationofArabidopsis

    This protocol is adapted from protocols by Nicole Bechtold (Bechtold et al. 1993), Andrew Bent (Bent et al. 1994) and Takashi Araki. No claims are made that any of the steps are necessary or ideal; these experiments have not been done. However, this protocol gives us very good results, with at least 95% of all infiltrated plants giving rise to transformants, and a transformant rate of 1-4% of seed. 1. So......閱讀全文

    In-Planta-Transformation-of-Arabidopsis

    實驗概要? ? ? ? A breakthrough in Arabidopsis research was the invention ofthe vacuum-infiltration procedure, a simple and reliable methodof obtaining

    Transformation-Protocol-for-Arabidopsis

    Transformation Protocol for Arabidopsis – AbbreviatedGerminate seed in pots↓ 4 weeksStreak bacteria onto YM/MinA↓ 2-3 days 28°CSpray/dip bacterial sus

    Simplified-Arabidopsis-Transformation-Protocol

    實驗概要Our present protocol (Clough and Bent, 1998; modified from Bechtold et al. 1993) is extremely simple. We have found that the MS salts, hormone

    Simplified-Arabidopsis-Transformation-Protocol

    (Brief version for those who are familiar with the method)Steve Clough and Andrew Bent, University of Illinois at Urbana-Champaign.Our present proto

    Plastid-Transformation-for-Abiotic-Stress-Tolerance-in-Plants

    Abiotic stresses such as drought, salinity, and extreme temperatures are ?major limiting factors in plant growth and development and pose serious ?thr

    Green-lab-protocol-for-vacuum-infiltration-transformation-of-Arabidopsis

    This protocol is adapted from protocols by Nicole Bechtold (Bechtold et al. 1993), Andrew Bent (Bent et al. 1994) and Takashi Araki. No claims are

    Arabidopsis-gDNA-isolation

    This is a simple and fast protocol for the extraction of genomic DNA from Arabidopsis thaliana that works fine in PCR for simple amplicons. We only us

    Chemical-transformation

    Chemical transformationPreparation of chemically competent cellsHave the following solutions at 0-4 deg C:a) 100 mM MgCl2b) 100 mM CaCl2-15% glycerolc

    Lactobacillus-transformation

    OverviewThis page details a electrotransformation protocol for?Lactobacillus?bacteria, specifically?Lactobacillus delbruckii?subsp.?bulgaricus?and?Lac

    Spheroplast-Transformation

    MaterialsYPD platesYPD1 M sorbitol 182 g/l (Sigma S7547)2 M sorbitol 36.4 g/100 mlSCE (per liter)1 M sorbitol (182 g)100 mM citric acid trisodium salt

    Bacterial-transformation

    IntroductionTransformation is the process of introducing foreign DNA (e.g plasmids, BAC) into a bacterium. Bacterial cells into which foreign DNA can

    Cell-Suspension-Culture-of-Arabidopsis

    實驗概要Cell Suspension Culture of Arabidopsis?主要試劑10% (v/v) Household BleachCallus Induction Medium?? ? ?Gamborg's B5 Basal Medium?? ? ?0.5 g/liter M

    Arabidopsis-RNA-extraction-protocol

    1-2 g fresh material, freezer-dried, ground with 0.2g sand (if necessary), and then homogenized with 10ml RNA extraction buffer (see below).Spin at 8,

    Arabidopsis-RNA-extraction-protocol

    1-2 g fresh material, freezer-dried, ground with 0.2g sand (if necessary), and then homogenized with 10ml RNA extraction buffer (see below). Spin

    Fast-Yeast-Transformation

    Protocol: Fast yeast transformationAdd 50 μl carrier DNA to a 1.5 ml tube.scrap cells from plate and add to the carrier DNA.Add in the following order

    High-Efficiency-Transformation

    Day 0Make sure you have the necessary solutions (instructions for how to make them can be found here):Single-stranded carrier DNAPEG 3350 50% w/vol1.0

    Method:-Lymphocyte-Transformation

    Method: Lymphocyte TransformationMay 30, 1990Rosalie VeilePrinciple:Lymphocytes are transformed to establish cell lines. Mononuclear cells (lymphocyte

    Agrobacterium-growth-and-transformation

    Growth and storage of Agrobacterium tumefaciensStrain GV3101: resistant to gentamycin and rifampicin so add 25-50 ug/ml Gentamycin, 10 ug/ ml rifampic

    Modified-Yeast-Transformation

    Inoculate cells from an overnight culture into 50 ml YEPD and incubate at 30°C with shaking. Typically, add 0.1 to 0.2 ml saturated culture in the eve

    ChIP-using-plant-samples-–-Arabidopsis

    實驗概要This protocol describes how chromatin is prepared from Arabidopsis, which can subsequently be used for chromatin immunoprecipitation (ChIP). T

    Production-of-Antibody-Fragments-in-Arabidopsis-Seeds

    Plants offer a number of attractive benefits over conventional mammalian or bacterial cell culture systems for the production of valuable pharmace

    Biosynthesis-of-Chorismate-in-Bacteria-and-Plants

    The biosynthesis of all three aromatic amino acids (tryptophan, tyrosine and phenylalanine) begins with the metabolic intermediate chorismate. The bio

    Biosynthesis-of-Tryptophan-in-Bacteria-and-Plants

    The aromatic amino acid tryptophan is an essential nutrient, meaning that humans and animals do not themselves have the biosynthetic machinery to synt

    L.-acidophilus-transformation

    OverviewElectrotransformation procedure for?Lactobacillus acidophilusProcedurePrepare Electrocompetent cellsInoculate overnight culture at 10^6 CFU/ml

    Streptomyces:Protocols/Transformation-by-Electroporation

    Description?Transform?E.coli?cells with plasmid/cosmid DNA using the method of electrophoration (inserting plasmids into?E.coli).Approx. Duration:Prep

    基因轉型(gene-transformation)

    目的帶有特定基因的質體在分子生物研究上,是一個很重要的工具,將質體送入細菌的過程稱為基因轉形,經由基因轉型可使質體在細菌中大量復制,以備進一步研究。本實驗將把你在前面轉殖實驗中cDNA和質體DNA的連結反應送入細菌。 你將從本實驗學習如何進行基因轉型作用。原理早在1970年左右,有人發現細菌經由冰冷

    In-Vitro-Conservation-and-Cryopreservation-of-Ornamental-Plants

    Today, the conservation of ornamental germplasm can take advantage of innovative techniques which allow preservation in vitro (slow growth storage

    Transformation-of-Magnaporthe-grisea-to-phosphinothricin-resistance

    Three transformation systems have been reported for the rice blast fungus?Magnaporthe grisea?(Parsons et al. 1987 Proc. Natl. Acad. Sci. USA 84:4161-4

    Transformation-of-E.-coli-by-Electroporation

    實驗概要? ? ? ? Electrocompetent bacteria are prepared by growing cultures to mid-log phase, washing the bacteria extensively at low?temperature, and

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