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FITC Armenian Hamster Anti-Mouse CD272 Antibody (6A6)

FITC Armenian Hamster Anti-Mouse CD272 Antibody (6A6)

Catalog Number: S0B80142 Application: FCM Reactivity: Ms Conjugation: FITC Brand: Starter
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Regular price $85 USD
Regular price Sale price $85 USD
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Product Details

Product Specification


Host Armenian hamster
Antigen CD272
Synonyms B- and T-lymphocyte attenuator; B- and T-lymphocyte-associated protein; Btla
Location Cell membrane
Accession Q7TSA3
Clone Number 6A6
Antibody Type Recombinant mAb
Isotype IgG
Application FCM
Reactivity Ms
Positive Sample C57BL/6 mouse splenocytes
Purification Protein G
Concentration 0.5 mg/ml
Conjugation FITC
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 1μg per million cells in 100μl volume Ms

Background

CD272, also known as B- and T-lymphocyte attenuator (BTLA), is an inhibitory receptor belonging to the CD28 immunoglobulin superfamily. It is encoded by the BTLA gene and primarily expressed on B cells, T cells, macrophages, and dendritic cells. BTLA plays a crucial role in regulating immune responses by acting as a negative regulator of antigen receptor signaling. Its ligand is HVEM (herpesvirus entry mediator, also known as CD270), and their interaction inhibits T cell and B cell activation, proliferation, and cytokine production. Structurally, BTLA is similar to other immune checkpoint proteins like PD-1 and CTLA-4, containing an extracellular IgV-like domain and intracellular immunoreceptor tyrosine-based inhibitory motifs (ITIMs) that mediate its inhibitory functions. BTLA's signaling involves the recruitment of tyrosine phosphatases SHP-1 and SHP-2, which dampen immune activation. Due to its role in immune regulation, the BTLA-HVEM axis is considered a promising target for cancer immunotherapy.

Picture

FC

Flow cytometric analysis of mouse CD272 expression on C57BL/6 mouse splenocytes. C57BL/6 mouse splenocytes were stained with Pacific Blue™ Rat Anti-Mouse CD45R/B220 Antibody and either FITC Armenian hamster IgG Isotype Control (left panel) or SDT FITC Armenian Hamster Anti-Mouse CD272 Antibody (right panel) at 2 μl/test. Total viable cells, as determined by Fixable Viability Dye 662 (S0D0016), were used for analysis. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.