Cluster of Differentiation 16 (CD16) Antibody (APC / Cyanine 7)

Este producto es parte de FCGR3A - Fc gamma receptor IIIa
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468€ (100 tests)

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935106861
info@markelab.com
name
Cluster of Differentiation 16 (CD16) Antibody (APC / Cyanine 7)
category
Primary Antibodies
provider
Abbexa
reference
abx140940
tested applications
FCM

Description

Cluster of Differentiation 16 (CD16) Antibody (APC / Cyanine 7) is a Mouse Monoclonal against Cluster of Differentiation 16 (CD16).

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Cluster of Differentiation 16 (CD16)
Host
Mouse
Reactivity
Human, Monkey
Clonality
Monoclonal
Conjugation
APC / Cyanine 7
Isotype
IgG1 Kappa
Clone ID
C307
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
Alias
CD16,FCG3,CD16A,FCGR3,IGFR3,IMD20,FCR-10,FCRIII,CD16-II,FCGRIII,FCRIIIA,FcGRIIIA,Low affinity immunoglobulin gamma Fc region receptor III-A,IgG Fc receptor III-A,IgG Fc receptor III-2
Background
Antibody anti-FCGR3A
Status
RUO

Descripción

FCGR3A, or Fc gamma receptor IIIa, is a membrane-bound protein that plays a crucial role in the immune system, specifically in mediating immune responses through the recognition of the Fc region of IgG antibodies. This receptor is primarily expressed on the surface of natural killer (NK) cells, macrophages, monocytes, and dendritic cells, where it facilitates antibody-dependent cellular cytotoxicity (ADCC) and other immune responses. It is part of the broader family of Fc gamma receptors (FcγRs), which are responsible for binding to the Fc region of IgG antibodies, thereby linking humoral and cellular immunity. FCGR3A has garnered considerable attention in immunology due to its role in recognizing and responding to immune complexes, infected cells, and tumor cells coated with IgG antibodies. Variations in the gene encoding FCGR3A have been implicated in differential responses to infections, autoimmune diseases, and cancer therapies

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