catalog number :
MBS214405
products full name :
MOUSE ANTI HUMAN C1q
products short name :
C1q
other names :
complement C1q subcomponent subunit A; Complement C1q subcomponent subunit A; complement C1q subcomponent subunit A; complement component 1, q subcomponent, alpha polypeptide; complement component C1q, A chain; complement component 1, q subcomponent, A chain
other gene names :
C1QA; C1QA
uniprot entry name :
C1QA_HUMAN
form :
Purified. Purified IgG - liquid
concentration :
Approximate Protein Concentration: 1.0 mg/ml
storage stability :
Store at 4 degree C or at -20 degree C if preferred. Storage in frost-free freezers is not recommended. This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use. Shelf Life: 18 months from the date of despatch.
tested application :
Immunohistology Frozen, ELISA (EIA), Flow cytometry (FC/FACS), Immunofluorescence (IF), Western Blot (WB)
app notes :
Immunohistology: For best results MyBioSource recommend HISTAR detection kits. Immunohistology - Frozen: Minimum Dilution: 1:500; Maximum Dilution: 1:1000
other info1 :
Perservative Stabilisers: 0.09% Sodium Azide (NaN3) . Preparation: Purified IgG prepared by affinity chromatography on Protein A
other info2 :
Histology Positive Control Tissue: Kidney from patients with streptococcal glomerulonephritis. Buffer Solution: Borate buffered saline. Target Species: Human
products description :
Mouse anti human C1q antibody, clone 3R9/2, recognizes human complement component 1 q (C1q), a 156kDa secreted protein. C1q associates with proenzymes C1r and C1s to form the calcium-dependent C1 complex, the first component of the serum complement system. C1q is composed of six A-, six B-chains and six C-polypeptide chains. Each chain contains a collagen-like region located near the N-terminus and a C-terminal globular region. These regions bind the Fc region of IgM and IgG molecules, initiating the classical pathway of complement activation. C1q deficiency has been associated with lupus erythematosus and glomerulonephritis (Troedson et al. 2013).
ncbi acc num :
NP_057075.1
ncbi gb acc num :
NM_015991.2
ncbi mol weight :
26,017 Da
ncbi pathways :
Chagas Disease (American Trypanosomiasis) Pathway 147809!!Chagas Disease (American Trypanosomiasis) Pathway 147795!!Classical Antibody-mediated Complement Activation Pathway 106409!!Complement Activation, Classical Pathway 198823!!Complement And Coagulation Cascades Pathway 198880!!Complement And Coagulation Cascades Pathway 83073!!Complement And Coagulation Cascades Pathway 484!!Complement Cascade Pathway 106405!!Creation Of C4 And C2 Activators Pathway 106407!!Immune System Pathway 106386
ncbi summary :
This gene encodes a major constituent of the human complement subcomponent C1q. C1q associates with C1r and C1s in order to yield the first component of the serum complement system. Deficiency of C1q has been associated with lupus erythematosus and glomerulonephritis. C1q is composed of 18 polypeptide chains: six A-chains, six B-chains, and six C-chains. Each chain contains a collagen-like region located near the N terminus and a C-terminal globular region. The A-, B-, and C-chains are arranged in the order A-C-B on chromosome 1. This gene encodes the A-chain polypeptide of human complement subcomponent C1q. [provided by RefSeq, Jul 2008]