JamesHardwickCNBrCleavageProcedure

1. Immunoprecipitate the protein and run it on a preparative gel. CNBr cleavage must be done with protein transferred to a nitrocellulose filter. Neither Immobilon nor Nylon can substitute.IMPORTANT: Wash the NC 2X for 15 min in deionized H2O after the transfer is complete. This removes any residual Tris-glycine that seems to affect the migration of the CNBr fragments during SDS-PAGE.2. Cut out the piece of......阅读全文

James-Hardwick-CNBr-Cleavage-Procedure

1. Immunoprecipitate the protein and run it on a preparative gel. CNBr cleavage must be done with protein transferred to a nitrocellulose filter. Neit

James-Hardwicks-angiotensin-assay-protocol

 This specific procedure was developed to assay the activity of the Lck kinase expressed from a retroviral vector in rat fibroblasts. You can obviousl

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Angiotensin-Protein-Kinase-Assay

James Hardwick's angiotensin assay protocolThis specific procedure was developed to assay the activity of the Lck kinase expressed from a retrovir

免疫疗法大牛James--:PD1抗体与CTLA4抗体原来如此不同

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Thrombin-Cleavage-of-GSTFusion-protein

INTRODUCTIONIn many cases the cleavage can be performed using the free intact fusion, or in same cases with the fusion protein bound to a matrix. The

Factor-Xa-Cleavage-of-MBPFusion-protein

INTRODUCTIONIn many cases the cleavage can be performed using the free intact fusion, or in same cases with the fusion protein bound to a matrix. The

Gramstaining-Procedure

Gram-staining is a four part procedure which uses certain dyes to make a bacterial cell stand out against against its background. The specimen should

TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS

Materials8% (w/v) paraformaldehyde stock solution:  Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high

DNA-EXTRACTION-PROCEDURE--GENERAL

Grow cells overnight in 500 ml broth medium.Pellet cells by centrifugation, and resuspend in 5 ml 50 mM Tris (pH 8.0), 50 mM EDTA.Freeze cell suspensi

TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS

Materials8% (w/v) paraformaldehyde stock solution:  Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high

In-Vivo-Luciferin-Imaging-Procedure

Mice are injected by an intraperitoneal route with a Luciferin solution (15 mg/mL or 30 mg/kg, in PBS, dose of 150 mg/kg) that is allowed to distribut

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement

IntroductionApoptosis is a normal physiological phenomenon put forward by Kerr [1]. It plays an important role in embryonic development, maintenance o

A-simple,-rapid-procedure-for-the-isolation-of-DNA-for-PCR

The polymerase chain reaction (PCR) is a method for amplifying specific segments of DNA defined by the small primers used to start the reaction. Using

A-simple,-rapid-procedure-for-the-isolation-of-DNA-for-PCR

N.M. DuTeau and J.F. Leslie - Department of Plant Pathology, Throckmorton Hall, Kansas State University, Manhattan, KS 66506-5502The polymerase chain

分子克隆蛋白表达实验指南(十一)

SDS-PAGE胶样品排列:        MarkerUII 37CUI’I’        Marker:低分子量蛋白marker,上样10ul        UI:未诱导菌液,上样10ul。任取37C和20C中一个        I:诱导后对照,上样10ul        UI’, I’代表G

Staining-Procedure-for-Flow-Cytometric-Detection-of-Human-Cyclins

Staining Procedure for Flow Cytometric Detection of Human CyclinsThis is a standard protocol used at Pharmingen for Quality Control testing of the ant

An-Integrative-Procedure-for-Apoptosis-Identification-and-Measurement2

TroubleshootingCritical Steps(1) Don’t trypsinize cells for too long when collecting them.(2) Rotation speed should be no more than 1500 rpm during ce

Standard-CellTrace™-Violet-TCell-Procedure

实验概要The CellTrace™  Violet Cell Proliferation Kit provides a versatile and well-retained  cell tracing reagent in a convenient and easy-to-use form. T

Keratocyte-isolation-(corneal-fibroblasts)

Corneal keratocytes (corneal fibroblasts) that this corneal layer is specialized fibroblasts residing in the stroma, representing about 85-90% of

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Tunel-Procedure-in-Bovine-Embryos-牛胚胎TUNEL检测凋亡

Materials8% (w/v) paraformaldehyde stock solution: Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go highe

DIRECT-AND-SHORTTERM-PROCEDURE-FOR-HARVESTING-BONE-MARROW-CHROMOSOMES

I. PurposeTo identify chromosome anomalies in hematopoietic cells. Used especially for chromosome studies for hematological disorders such as preleuke

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