PerCP-Cyanine5.5 - anti Mouse CD152 - UC10-4F10-11

PerCP-Cyanine5.5 - anti Mouse CD152 - UC10-4F10-11

Catalog Number:
A001109538IMM
Mfr. No.:
MO152PP5.5(V25); MO152PP5.5(V100)
Price:
$288
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      • Overview
        • CD152 also known as, Cytotoxic T-lymph ocyte-associated antigen 4 (CTLA-4). CD152 is expressed on activated T lymph ocytes 2-3 days after stimulation through T cell receptor. CTLA-4 has significant similarity to CD28 in amino acid sequence, structure, and genomic organization. Furthermore, CD152 and CD28 share common B7 family counter-receptors. Unlike CD28, CD152 expression appears to be restricted to activated T cells and CD25+CD4+ regulatory T (Treg) cells. Whereas CD28 delivers a costimulatory signal required for T-cell activation, CTLA-4 is a negative regulator of cell-mediated immune responses. CD152 may play roles in induction and/or maintenance of immunological tolerance, regulation of protective immunity, and autoimmune responses, and regulation of some aspects of thymocyte maturation. This hamster mAb to a mouse leukocyte antigen does not cross-react with rat leucocytes.

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      • Properties
        • Host
          armenian hamster
          Isotype
          IgG
          Reactivity
          mouse
          Clone
          UC10-4F10-11
          Immunogen
          Mouse CTLA-4 IgG2a Fusion
          Conjugate
          PerCP/Cyanine5.5
          Storage
          Store in the dark at 2-8 °C
          Concentration
          0.2 mg/ml
          Molecular Weight
          33 kD
          Regulatory Status
          RUO
          Antigen
          Ctla4; CTLA-4; Cytotoxic T-lymph ocyte-associated protein 4; Ly-56 (Gene ID:12477)

          * For research use only.

      • Applications
        • Application
          Flow Cytometry
          Application Description
          CD152, clone UC10-AF10-11, is a mAb intended for RUO in the identification/enumeration of lymph that express CD152. This reagent is effective for direct IF staining of mouse sample for FCM analysis using ≤1 µg/106 cells.

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