CFHR5 (NM_030787) Human Recombinant Protein
Product Specifications
Background
This gene is a member of a small complement factor H (CFH) gene cluster on chromosome 1. Each member of this gene family contains multiple short consensus repeats (SCRs) typical of regulators of complement activation. The protein encoded by this gene has nine SCRs with the first two repeats having heparin binding properties, a region within repeats 5-7 having heparin binding and C reactive protein binding properties, and the C-terminal repeats being similar to a complement component 3 b (C3b) binding domain. This protein co-localizes with C3, binds C3b in a dose-dependent manner, and is recruited to tissues damaged by C-reactive protein. Allelic variations in this gene have been associated, but not causally linked, with two different forms of kidney disease: membranoproliferative glomerulonephritis type II (MPGNII) and hemolytic uraemic syndrome (HUS) . [provided by RefSeq, Jan 2010]
Synonyms
CFHL5; CFHR5D; FHR-5; FHR5
Gene ID
81494
UniProt
Q9BXR6
Accession Number mRNA
NM_030787
Chromosomal Location
1q31.3
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Secreted Protein, Transmembrane
Molecular Weight
62.5 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
CFHR5
Species
Human
Protein ID
NP_110414
Overview
Recombinant protein of human complement factor H-related 5 (CFHR5)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/81494
Uniprot URL
https://www.uniprot.org/uniprot/Q9BXR6
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_030787
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_110414
Curated Selection
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