Human Fc Fragment Of IgG Low Affinity IIIb Receptor (FCGR3B) Protein

Este producto es parte de FCGR3B - Fc gamma receptor IIIb
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234€ (2 µg)

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935106861
info@markelab.com
name
Human Fc Fragment Of IgG Low Affinity IIIb Receptor (FCGR3B) Protein
category
Proteins and Peptides
provider
Abbexa
reference
abx680179
tested applications
SDS-PAGE

Description

Human Fc Fragment Of IgG Low Affinity IIIb Receptor (FCGR3B) Protein is a recombinant protein produced in Sf9, Baculovirus cells.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryProteins and Peptides
Immunogen TargetFc Fragment Of IgG Low Affinity IIIb Receptor (FCGR3B)
HostInsect
OriginHuman
ConjugationUnconjugated
ExpressionRecombinant
Purity> 90% (SDS-PAGE)
Size 12 µg
Size 210 µg
Size 31 mg
FormLiquid
Tested ApplicationsSDS-PAGE
AvailabilityShipped within 5-10 working days.
Dry IceNo
AliasCD16,FCG3,CD16A,CD16b,FCGR3,CD16-I,FCGR3A,FCR-10,FCRIII,FCRIIIb,Low affinity immunoglobulin gamma Fc region receptor III-B,Fc-gamma RIII-beta,IgG Fc receptor III-1
BackgroundProtein FCGR3B
StatusRUO
NoteThis product is for research use only. Not for human consumption, cosmetic, therapeutic or diagnostic use.

Descripción

FCGR3B, or Fc gamma receptor IIIb, is a low-affinity receptor for the Fc portion of immunoglobulin G (IgG) antibodies, primarily expressed on neutrophils. It is a member of the Fc gamma receptor (FcγR) family, which plays a pivotal role in mediating immune responses through the recognition of the Fc region of IgG antibodies. FCGR3B is one of the two isoforms of FcγRIII, the other being FCGR3A (CD16A). While both isoforms share sequence similarity and belong to the same gene family, they have distinct tissue distributions, membrane anchoring mechanisms, and functional roles in the immune system. FCGR3B is especially important for facilitating immune complex clearance, phagocytosis, and neutrophil activation, processes that are crucial in maintaining immune homeostasis and defending against pathogens. Dysregulation of FCGR3B or mutations in its gene have been associated with a range of clinical conditions, including autoimmune diseases and chronic inflammatory disorders

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