Recombinant Human FCRL1 protein (His tag)
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Recombinant Human FCRL1 protein (His tag) is a Human Fragment protein, in the 1 to 303 aa range, expressed in HEK 293 cells, with >98%, < 1 EU/µg endotoxin level, suitable for SDS-PAGE.
View Alternative Names
CD307a, FCRH1, IFGP1, IRTA5, FCRL1, Fc receptor-like protein 1, FcR-like protein 1, FcRL1, Fc receptor homolog 1, IFGP family protein 1, Immune receptor translocation-associated protein 5, FcRH1, hIFGP1
- SDS-PAGE
Supplier Data
SDS-PAGE - Recombinant Human FCRL1 protein (His tag) (AB276402)
SDS-PAGE analysis of ab276402
Reactivity data
Sequence info
Properties and storage information
Form
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
FCRL1 serves an important role in modulating the B cell receptor (BCR) signaling. It does not form part of a larger receptor complex but interacts directly with components of the BCR. This interaction affects the activation thresholds of B cells helping to fine-tune immune responses. FCRL1 supports maintaining immune homeostasis by balancing the activation and inhibition of B cells.
Pathways
FCRL1 participates actively in the BCR signaling pathway and is involved in modulating the MAPK/ERK pathway. FCRL1 interacts with signaling molecules related to these pathways such as SHP-1 which can modulate downstream effects. By adjusting these signaling dynamics FCRL1 indirectly influences processes central to adaptive immune responses linking it to other receptor family members like FcγRs.
General info
Function
Type I transmembrane surface glycoprotein preferentially expressed by B-cells that regulates BCR-mediated signaling responses (PubMed : 15479727). Recruits ABL1 as the intracellular effector molecule to enhance B-cell activation (By similarity). Also plays a negative role by suppressing ERK activation under homeostatic and BCR-stimulated conditions in a GRB2-dependent manner (By similarity).
Post-translational modifications
Phosphorylated on tyrosines upon activation.
Target data
Product promise
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