Programmed Cell Death 1 Ligand 1 (CD274) Antibody (FITC)

364€ (100 tests)
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935106861
info@markelab.com
name
Programmed Cell Death 1 Ligand 1 (CD274) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx140489
tested applications
FCM
Description
CD274 Antibody (FITC) is a Mouse Monoclonal Antibody against CD274 conjugated to FITC.
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Programmed Cell Death 1 Ligand 1 (CD274) |
Host | Mouse |
Reactivity | Human, Monkey |
Recommended Dilution | FCM: 4 µl/100 µl of whole blood or 106 cells. Optimal dilutions/concentrations should be determined by the end user.The content of a vial (0.4 ml) is sufficient for 100 tests. |
Clonality | Monoclonal |
Conjugation | FITC |
Isotype | IgG2b Kappa |
Clone ID | E456 |
Size 1 | 100 tests |
Tested Applications | FCM |
Buffer | Stabilizing PBS solution containing 15 mM sodium azide. |
Availability | Shipped within 5-12 working days. |
Storage | Store in the dark at 2-8°C. Avoid exposure to light. Do not freeze. |
Dry Ice | No |
UniProt ID | Q9NZQ7 |
Gene ID | 29126 |
OMIM | 605402 |
Alias | B7-H,B7H1,PDL,PD-L1,hPD-L1,PDCD1L1,PDCD1LG1,B7 homolog 1,PDCD1 ligand 1,Programmed death ligand 1,Programmed cell death 1 ligand 1 |
Background | Antibody anti-CD274 |
Status | RUO |
Descripción
CD274 molecule, also known as Programmed Death-Ligand 1 (PD-L1), is a critical component in the immune checkpoint pathway. Encoded by the CD274 gene located on chromosome 9p24.1, PD-L1 is primarily expressed on the surface of various cell types, including immune cells (such as T cells, B cells, dendritic cells, and macrophages) and non-immune cells (including epithelial and endothelial cells). Its expression can be upregulated in response to inflammatory signals, particularly interferon-gamma (IFN-γ). PD-L1 plays a vital role in maintaining immune homeostasis and preventing autoimmunity by regulating the activity of T cells. PD-L1 gained significant attention in cancer immunotherapy due to its role in tumor immune evasion. Many tumors exploit the PD-1/PD-L1 pathway to suppress anti-tumor immune responses, allowing cancer cells to escape immune surveillance
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