CD134 Antibody (FITC)

104€ (20 tests)
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935106861
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name
CD134 Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx229302
tested applications
FCM
Description
CD134 Antibody (FITC) is a Human Monoclonal Antibody against CD134.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | CD134 |
Host | Mouse |
Reactivity | Human |
Clonality | Monoclonal |
Conjugation | FITC |
Isotype | IgG1 Kappa |
Size 1 | 20 tests |
Size 2 | 100 tests |
Size 3 | 200 tests |
Tested Applications | FCM |
Buffer | PBS with 0.05% Proclin300, 1% BSA. |
Availability | Shipped within 5-15 working days. |
Storage | Aliquot and store at 2°C to 8°C upon receipt. Avoid exposure to light. Do not freeze. |
Dry Ice | No |
UniProt ID | P43489 |
Gene ID | 7293 |
Alias | OX40,ACT35,CD134,IMD16,TXGP1L,OX40L receptor,TAX transcriptionally-activated glycoprotein 1 receptor |
Background | Antibody anti-TNFRSF4 |
Status | RUO |
Descripción
TNFRSF4, commonly known as OX40 (CD134), is a member of the tumor necrosis factor receptor (TNFR) superfamily. It is an important costimulatory molecule expressed on T cells, specifically induced upon T cell activation. TNFRSF4 is known for its involvement in regulating immune responses, especially in T-cell proliferation, survival, and memory formation. As an immune-regulatory receptor, it primarily interacts with its ligand, OX40L (TNFSF4), which is expressed on antigen-presenting cells (APCs), such as dendritic cells, B cells, and macrophages. OX40’s role in immune modulation is significant because it amplifies T-cell responses during both acute infections and in chronic immune responses, such as autoimmune diseases and cancer. By sustaining T-cell activation and enhancing immune memory, OX40 has become a central target in immunotherapy research, especially in the contexts of cancer immunotherapy and autoimmune diseases. Its ability to promote prolonged immune responses also makes it a critical regulator in various immune-related diseases, where modulation of OX40-OX40L interactions can potentially benefit patient outcomes.
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