Complement Factor H-Related Protein 5 (CFHR5) Antibody (HRP)

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260€ (50 µl)

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935106861
info@markelab.com
name
Complement Factor H-Related Protein 5 (CFHR5) Antibody (HRP)
category
Primary Antibodies
provider
Abbexa
reference
abx349316
tested applications
ELISA

Description

Complement Factor H-Related Protein 5 (CFHR5) Antibody (HRP) is a Rabbit Polyclonal antibody conjugated to HRP for the detection of Human CFHR5.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Complement Factor H-Related Protein 5 (CFHR5)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
HRP
Isotype
IgG
Purification
Purified by antigen affinity chromatography.
Size 1
50 µl
Size 2
100 µl
Size 3
200 µl
Size 4
1 ml
Form
Liquid
Tested Applications
ELISA
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9BXR6
Background
Antibody anti-CFHR5
Status
RUO

Descripción

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abx032588

Complement Factor H-Related Protein 5 (CFHR5) Antibody

CFHR5 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].

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