10182242

10182242
| Product Name | Anti-Human CD152,APC Flow Cytometry Antibody |
|---|---|
| Target | CTLA4, CD152, GSE |
| Label | APC |
| Instrument | Flow cytometer compatible with 633nm laser |
| Subtype | Mouse IgG2a, κ |
| Clone Number | BNI3 |
| Recommended Application | Flow cytometry |
| Dosage | 5 μL /Test |
| Purification | Affinity chromatography |
| Stock Solution | Phosphate buffer solution (pH7.2) containing 0.2% BSA and 0.2% proclin 950 |
| Storage Conditions | Store at 2 - 8℃, protect from light, do not freeze |

Figure-The results of Anti-Human CD3, FITC and Anti-Human CD152, APC(Clone: BNI3) staining in the control group (left) which was not stimulated by human heparin anticoagulation and the experimental group (right) which was blocked by PMA/Ionomycin overnight.
Overview of CTLA4 molecular target information
Molecular name: CTL A4, cytotoxic T-lympocyte associated protein 4.
Gene family: CD molecules; V-set domain containing
Alias: CD152; CD; GSE; CTLA-4
Former name: CELIAC3; IDDM12
Full name: celiac disease 3; insulin-dependent diabetes mellitus 12
Summary of molecular targets of CTLA4
Cytotoxic T lymphocyte associated protein 4 (CTLA-4), also known as CD152, is a member of immunoglobulin superfamily and expressed on the surface of helper T cells. CTLA-4 is similar to the costimulatory protein CD28 of T cells, and both of them bind to CD80 and CD86. CTLA-4 transmits inhibitory signals to T cells, while CD28 transmits stimulating signals. CTLA-4 can function as an immune checkpoint, down-regulate the immune system, and act as a "off" switch when it binds to CD80 or CD86 on the surface of antigen presenting cells. Intracellular CTLA-4 also exists in regulatory T cells, which is important for their function. The gene mutation is related to insulin-dependent diabetes, hyperthyroidism, Hashimoto's thyroiditis, celiac disease, systemic lupus erythematosus, thyroid-associated ophthalmopathy, primary biliary cirrhosis and other autoimmune diseases. The polymorphism of CTLA-4 gene is related to autoimmune diseases such as autoimmune thyroid diseases and multiple sclerosis, but the correlation is usually weak. In systemic lupus erythematosus (SLE), it is found that the splicing variant of soluble CTLA-4 is abnormally produced and exists in the serum of patients with the disease.