Rat anti-Mouse Complement C1q Monoclonal Antibody | anti-C1QC antibody

Complement C1q, Mouse (Biotin)

Cat. Num. AAA631845

• Gene Names: C1QC; C1QG; C1Q-C
• Reactivity: Mouse
• Applications: ELISA, Western Blot
• Purity: Purified; Purified.
• Synonyms: Complement C1q; Monoclonal Antibody; Mouse (Biotin); Anti -Complement C1q; anti-C1QC antibody

• Host: Rat
• Reactivity: Mouse
• Clonality: Monoclonal
• Isotype: IgG
• Clone Number: 9j111
• Specificity: Recognizes Mouse Complement C1q Antibodies.
• Purity/Purification: Purified; Purified.
• Form/Format: Supplied as a lyophillized powder in PBS, pH 7.4, 0.2% BSA, 0.05% sodium azide. Labeled with Biotin. Reconstitute in 250ul of PBS.

• Applicable Applications for anti-C1QC antibody: ELISA (EL/EIA), Western Blot (WB)
• Application Notes: Suitable for use in ELISA and Western Blot.; Dilution: ELISA: 1:10,000-1:50,000. Use 10-100ng of control antigen per well.; Western Blot: 1:1000 -1:5000 using ECL.
• Preparation and Storage: Lyophilized powder may be stored at -20 degree C. Stable for 12 months at -20 degree C. Reconstitute with sterile PBS. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Reconstituted product is stable for 12 months at -20 degree C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.

Related Product Information for anti-C1QC antibody

Acrp30 (adipocyte complement-related protein of 30kD), also known as AdipoQ, APM1, Adiponectin, Gelatin binding protein 28kD/GBP28 or adipocyte most abundant gene transcript) was identified as a novel adipocyte-specific synthesized and secreted protein with structural resemblance to complement factor C1q. Like adipsin, Acrp30 secretion is induced ~10-fold during adipocyte differentiation. Plasma levels are reduced in obese humans, and low levels are associated with insulin-resistance. C1q is serum glycoprotein of 18-polypeptides chains consisting of three non-identical subunits, A (29kD), B (26kD), and C (246aa, 19kD)

Product Categories/Family for anti-C1QC antibody

Antibodies; Abs to Complement

NCBI and Uniprot Product Information

• NCBI GI #: 166235903
• NCBI GeneID: 714
• NCBI Accession #: NP_001107573.1
• NCBI GenBank Nucleotide #: NM_001114101.1
• UniProt Accession #: P02747; Q7Z502; Q96DL2; Q96H05
• Molecular Weight: 25,774 Da
• NCBI Official Full Name: complement C1q subcomponent subunit C
• NCBI Official Synonym Full Names: complement component 1, q subcomponent, C chain
• NCBI Official Symbol: C1QC
• NCBI Official Synonym Symbols: C1QG; C1Q-C
• NCBI Protein Information: complement C1q subcomponent subunit C; complement component 1, q subcomponent, gamma polypeptide
• UniProt Protein Name: Complement C1q subcomponent subunit C
• Protein Family: Complement C1q-like protein
• UniProt Gene Name: C1QC
• UniProt Synonym Gene Names: C1QG
• UniProt Entry Name: C1QC_HUMAN

NCBI Description

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. A deficiency in 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 C-chain polypeptide of human complement subcomponent C1q. Alternatively spliced transcript variants that encode the same protein have been found for this gene. [provided by RefSeq, Jul 2008]

Uniprot Description

C1QC: C1q associates with the proenzymes C1r and C1s to yield C1, the first component of the serum complement system. The collagen-like regions of C1q interact with the Ca(2+)-dependent C1r(2)C1s(2) proenzyme complex, and efficient activation of C1 takes place on interaction of the globular heads of C1q with the Fc regions of IgG or IgM antibody present in immune complexes. Defects in C1QC are a cause of complement component C1q deficiency (C1QD). A rare defect resulting in C1 deficiency and impaired activation of the complement classical pathway. C1 deficiency generally leads to severe immune complex disease with features of systemic lupus erythematosus and glomerulonephritis.

Protein type: Secreted, signal peptide; Secreted

Chromosomal Location of Human Ortholog: 1p36.11

Cellular Component: extracellular space; collagen; extracellular region

Biological Process: negative regulation of macrophage differentiation; innate immune response; immune response; complement activation, classical pathway; complement activation; negative regulation of granulocyte differentiation

Disease: C1q Deficiency