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YL Biont

YLBiont

YL Biont is a combination of research &  production as one of the leading international biological high-tech enterprises.

The company is focused on immune detection reagents of independent research and development, the main products include ELISA kits, CLIA kits, proteins, antibodies, mark kits and other related reagents, with a total of more than 20.000 products! Through the national support and new high-tech industries promoted, they have advanced production technology in the field of biological kits. The YL company will continue to do research and development, improving competition of their products' quality. At the same time, the products of research and development face the market at home and abroad.

YL Biont pursues "integrity, dedication, innovation and win-win" as our spirit of enterprise, which is devoted to building a first-class team and providing customers first-class products.
www.ylbiont.com

Rabbit anti-Semaphorin 4A Antibody YLD7053

YLbiont_Antibody.jpg


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Specifications

50ul / 100ul price = 100ul

Clonality:

Polyclonal

Synonyms:

SEMAB; SEMB; Semaphorin-4A; Semaphorin-B; Sema B

Host:

Rabbit

Reactivity:

Human, Monkey

Applications:

WB, IF/IC, IP

Background:

Rabbit polyclonal antibody to Semaphorin 4A

Immunogen:

KLH-conjugated synthetic peptide encompassing a sequence within the center region of human Semaphorin 4A. The exact sequence is proprietary.

Purification method:

The antibody was purified by immunogen affinity chromatography.

Concentration:

1mg/mL

Buffer:

Liquid in 0.42% Potassium phosphate, 0.87% Sodium chloride, pH 7.3, 30% glycerol, and 0.01% sodium azide.

Dilution:

WB (1/500 - 1/1000), IF/IC (1/100 - 1/500), IP (1/10 - 1/100)

Conjugation:

WB description:

Western blot analysis of Semaphorin 4A expression in HeLa (A), COS7 (B) whole cell lysates.

IHC description:

IF/ICC description:

Immunofluorescent analysis of Semaphorin 4A staining in HeLa cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the primary antibody in 3% BSA-PBS and incubated overnight at 4 °C in a humidified chamber. Cells were washed with PBST and incubated with a DyLight 594-conjugated secondary antibody (red) in PBS at room temperature in the dark. DAPI was used to stain the cell nuclei (blue).

IP description:

Immunoprecipitation of Semaphorin 4A from 0.5mg Jurkat whole cell extract lysate, using 5ug of anti-Semaphorin 4A Antibody and 50ul of protein G magnetic beads (+). No antibody was added to the control (-). The antibody was incubated under agitation with Protein G beads for 10min, Jurkat whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation. Proteins were eluted by addition of 40ul SDS loading buffer and incubated for 10min at 70°C; 10ul of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with anti-Semaphorin 4A Antibody.

FC description:

ChIP description

Storage:

Store at -20℃. Avoid repeated freeze / thaw cycles.