丁香实验_LOGO
登录
提问
我要登录
|免费注册
丁香实验推荐阅读
Lethal phase determination

Lethal phase determination1. Pick a bunch of heterozygote L4 hermaphrodites to a new plate.2. The next day there will be eggs on the plate; pick exactly 20 of these to each of a few plates. Make sure ...

丁香实验推荐阅读
Integrating extrachromasomal arrays into the C. elegans chromosomes

Integrating extrachromasomal arrays into the C. elegans chromosomesWhy and how to do itby Michael Koelle12/20/94What is the benefit of integrating an extrachromosomal array? Extrachromosomal arrays su ...

丁香实验推荐阅读
Microinjecting worms

Microinjecting worms by Michael Koelle8/23/94You will have a couple frustrating sessions when you first attempt this technique but everyone seems to master injection after a few days and it works very ...

丁香实验推荐阅读
Generating males by heat shock

Generating males by heat shockby Michael Koelle1. Set up ~6 plates with 5 L4 hermaphordites each.2. Heat shock 4-6 hours at 30°. 8-9 hours works but gives few progeny.3. Return to 20°. Should get a fe ...

丁香实验推荐阅读
LIQUID CULTURE OF WORMS WITH FERMENTOR

LIQUID CULTURE OF WORMS WITH FERMENTORMimi H. Zhou Hsiuchin Yang Bill Walthall Biology Department Georgia State University Atlanta GA 30302 The yield of C. elegans and their food (E.coli) are relative ...

丁香实验推荐阅读
Liquid culture of worms

Liquid culture of wormsBy Michael Koelle and Tory Herman adapted from Mir Hengartner4/6/94Media1) superbroth (5 X 2 1/2 liters autoclaved in 6 liter flasks) 5 X 30 g Bactotryptone 5 X 60 g yeast extra ...

丁香实验推荐阅读
Single Worm PCR

Single Worm PCRReagents:Lysis Buffer: 50 mM KCl10 mM Tris pH 8.32.5 mM MgCl20.45% NP-40 (IGEPAL)0.45% Tween-200.01% Gelatin Proteinase K: 20 mg/ml 10X PCR Buffer: 100 mM Tris 500 mM KCl 15 mM MgCl2 pH ...

丁香实验推荐阅读
snip-SNP mapping with CB4856 polymorphisms

snip-SNP mapping with CB4856 polymorphismsMaterials:Worm Lysis Buffer PCR reagents PCR primers flanking a SNP 2X restriction mix with the appropriate enzyme Procedure:Generate recombinant lines for th ...

丁香实验推荐阅读
Synchronizing Worm Cultures

Synchronizing Worm CulturesSynchronization is based on the fact newly hatched larvae will live but not develop if deprived of a food source. An asynchronous population of embryos is isolated and then ...

丁香实验推荐阅读
N2 development times at different temperatures

N2 development times at different temperaturesby Michael KoelleDetermined empirically; times in hours are given from the first division of the zygote.15°20°25°eggs laid217hatch22139L1 molt492921L2 mo ...

丁香实验推荐阅读
low frequency table

low frequency tableCodon usage for C. elegans lowly biased (lowly expressed by inference) genes. (Stenico M. Lloyd A. T. and Sharp P. M. (1994). Nucleic Acids Research 22: 2437-2246 AmAcidCodonNumber/ ...

丁香实验推荐阅读
Worm genomic Southern blots

Worm genomic Southern blotsby Michael Koelle4/6/94I. Preparing worm genomic DNA: requires 1-2 days to seed agarose plates a few days for the worms to grow 1-2 days to prep the DNA1. Seed large agarose ...

丁香实验推荐阅读
Worm PCR

Worm PCRPick one worm and place it in a 2.5 l drop of lysis buffer in the cap of a PCR tube. Close and centrifuge briefly to move to the bottom of the tube. Freeze the tubes at -70°C for 15 min. The ...

丁香实验推荐阅读
Genomic DNA prep

Genomic DNA prep(Jorgensen Lab ) Make worm growth plates. These use agarose to avoid impurities in most batches of agar and are enriched to allow greater worm growth. Mix:5 g Bacto tryptone2 g Bacto y ...

丁香实验推荐阅读
Joe mRNA prep

Joe's mRNA prep(Audrey Gasch Pat Brown ) Oligo-dT cellulose prepDump Ambion vial contents into 50 ml c/f tube Add 10 ml 1x NETS to vial cap rinse vial dump 10 ml into c/f tube Spin tube 3000 rpm 2 min ...

丁香实验推荐阅读
Yale RNA prep

Yale RNA prep(Rebecca D. Burdine Michael J. Stern ) Add 8 ml of TRIZOL to 2 ml packed worms in 15 ml centrifuge tube. Vortex and invert tube to solubilize and lyse worms for at least 10 min. Divide in ...

丁香实验推荐阅读
Antibody Staining of Dissected Gonads

Antibody Staining of Dissected Gonads - From R. Francis - -Adapted by Min-Ho Lee-Antibody staining (in Tubes) 1. Using a pasteur pipette (drawn in flame and cut open) transfer worm carcasses with a ...

丁香实验推荐阅读
RUVKUN Antibody Staining Protocol revised 10/29/90

RUVKUN Antibody Staining Protocol revised 10/29/90Fixation: 1. C. elegans N2 grown in liquid or plates. Harvest worms.Wash for 2 hours at room temp. in 1X M9 or PBS. 2. Fix in 5 ml of FRESH THAT DAY 1 ...

丁香实验推荐阅读
C. elegans whole mount immunohistochemistry with Bouin Fixative

C. elegans whole mount immunohistochemistry with Bouin's FixativeI have developed a fixation protocol which provides an alternative set of conditions to test antisera that work poorly on paraformaldeh ...

丁香实验推荐阅读
DAPI Staining

DAPI Staining To visualize DNA incubate fixed samples with 100 ng/ml 4'6'-diamidino-2-phenylindole hydrochloride (DAPI) in PBS for 30 min. Rinse 3x with PBTw. MaterialsPBS: Sambrook et al. (Molecular ...

提问
扫一扫
丁香实验小程序二维码
实验小助手
丁香实验公众号二维码
扫码领资料
反馈
TOP
打开小程序