Flow cytometry Anti-bodies Human

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CDX2 Product

Get tips on using CDX2 to perform Immunohistochemistry Human - CDX2

Products BIOCARE MEDICAL CDX2

Get tips on using lenti MS2-P65-HSF1_Hygro to perform CRISPR Human - Activation PDIA1

Products Addgene lenti MS2-P65-HSF1_Hygro

Get tips on using lenti MS2-P65-HSF1_Hygro to perform CRISPR Human - Activation APOBEC3G

Products Addgene lenti MS2-P65-HSF1_Hygro

Get tips on using pcDNA-dCas9-p300 Core to perform CRISPR Human - Activation MASPIN

Products Addgene pcDNA-dCas9-p300 Core

Get tips on using pAC2-dual-dCas9VP48-sgExpression to perform CRISPR Human - Activation IL1RN

Products Addgene pAC2-dual-dCas9VP48-sgExpression

Get tips on using UltraCruz® Transfection Reagent to perform CRISPR Human - Activation GRP78

Products Santa Cruz Biotechnology UltraCruz® Transfection Reagent

Get tips on using pAC2-dual-dCas9VP48-sgExpression to perform CRISPR Human - Activation SOX2

Products Addgene pAC2-dual-dCas9VP48-sgExpression

Western blotting is a widely used technique to size separate proteins from a pool of cell or tissue lysates. The technique has 4 major steps: a) gel electrophoresis, b) blocking and treatment with antigen specific antibody, c) treatment with secondary antibody and finally d) detection and visualization. Though western blotting is a widely used technique, detection of specific proteins depends on several factors, the major ones are antibody concentration, incubation time and washing steps. Key points for obtaining clean blots are: always prepare fresh buffer solutions and optimize antibody concentration. Given the advent of high-throughput protein analysis and a push to limit the use of lab consumables, onestep antibodies are developed which recognise protein of interest and also contain a detection label.

Proteins Western blotting Cytochrome C

Western blotting is a widely used technique to size separate proteins from a pool of cell or tissue lysates. The technique has 4 major steps: a) gel electrophoresis, b) blocking and treatment with antigen specific antibody, c) treatment with secondary antibody and finally d) detection and visualization. Though western blotting is a widely used technique, detection of specific proteins depends on several factors, the major ones are antibody concentration, incubation time and washing steps. Key points for obtaining clean blots are: always prepare fresh buffer solutions and optimize antibody concentration. Given the advent of high-throughput protein analysis and a push to limit the use of lab consumables, onestep antibodies are developed which recognise protein of interest and also contain a detection label.

Proteins Western blotting EGFR

Western blotting is a widely used technique to size separate proteins from a pool of cell or tissue lysates. The technique has 4 major steps: a) gel electrophoresis, b) blocking and treatment with antigen specific antibody, c) treatment with secondary antibody and finally d) detection and visualization. Though western blotting is a widely used technique, detection of specific proteins depends on several factors, the major ones are antibody concentration, incubation time and washing steps. Key points for obtaining clean blots are: always prepare fresh buffer solutions and optimize antibody concentration. Given the advent of high-throughput protein analysis and a push to limit the use of lab consumables, onestep antibodies are developed which recognise protein of interest and also contain a detection label.

Proteins Western blotting p53

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