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PercP-Cy5.5 Mouse Anti-Rat CD4 Antibody (S-R631)

PercP-Cy5.5 Mouse Anti-Rat CD4 Antibody (S-R631)

Catalog Number: S0B5460 Application: FCM Reactivity: Rat Conjugation: PerCP-Cy5.5 Brand: Starter
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Regular price $125 USD
Regular price Sale price $125 USD
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Product Details

Product Specification


Host Mouse
Antigen CD4
Synonyms T-cell surface glycoprotein CD4; T-cell surface antigen T4/Leu-3; W3/25 antigen
Location Cell membrane
Accession P05540
Clone Number S-R631
Antibody Type Mouse mAb
Isotype IgG1,k
Application FCM
Reactivity Rt
Positive Sample SD Rat splenocytes
Purification Protein G
Concentration 0.05mg/ml
Conjugation PerCP-Cy5.5
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage 12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.

Dilution


application dilution species
FCM 5μl per million cells in 100μl volume Rt

Background

CD4 is a glycoprotein expressed on the surface of certain immune cells, most notably helper T cells. It is a member of the immunoglobulin superfamily and has four immunoglobulin-like domains (D1 to D4). CD4 acts as a co-receptor with the T-cell receptor (TCR) to recognize antigens displayed by MHC class II molecules on antigen-presenting cells. The D1 domain of CD4 binds to the β2 region of MHC class II, bringing the TCR complex and CD4 into close proximity. This allows the tyrosine kinase Lck, bound to the cytoplasmic tail of CD4, to phosphorylate tyrosine residues on the cytoplasmic domains of CD3, amplifying the signal generated by the TCR. CD4 is also the primary receptor for the human immunodeficiency virus (HIV), and its interaction with the HIV gp120 protein is a key step in viral entry.

Picture

FC

Flow cytometric analysis of Rat CD4 expression on SD Rat splenocytes. SD Rat splenocytes were stained with Brilliant Violet 605™ Mouse Anti-Rat CD3 Antibody and either PercP-Cy5.5 Mouse IgG1, κ Isotype Control (Left panel) or SDT PercP-Cy5.5 Mouse Anti-Rat CD4 Antibody (Right panel) at 5 μl/test. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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