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C1q-C Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT0565
产品名称
C1q-C Rabbit Polyclonal Antibody
别名
C1QC; C1QG; Complement C1q subcomponent subunit C
类别
常规抗体
基因名称
C1QC
蛋白名称
Complement C1q subcomponent subunit C
推荐应用
WB
反应种属
Human,Mouse,Rat
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
714
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=714
Human Swissprot No.
P02747
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P02747/entry
Mouse Gene ID
12262
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=12262
Mouse Swissprot No.
Q02105
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q02105
Rat Gene ID
362634
Rat Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=362634
Rat Swissprot No.
P31722
Rat Swissprot Link
http://www.uniprot.org/uniprot/P31722
免疫原
The antiserum was produced against synthesized peptide derived from human C1QC. AA range:81-130
特异性
C1q-C Polyclonal Antibody detects endogenous levels of C1q-C protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
预测分子量
30kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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],
组织表达
Brain,Cerebellum,Monocyte,
细胞定位
Secreted.
信号通路
Complement and coagulation cascades;Prion diseases;Systemic lupus erythematosus;
功能
disease:Defects in C1QC are a cause of C1q deficiency [MIM:120575]. It is a rare genetic disorder which is associated with recurrent infections and a high prevalence of lupus erythematosus-like symptoms. It is characterized by a loss of activation of the complement classical pathway.,function: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.,online information:C1QC mutation db,PTM:O-linked glycans consist of Glc-Gal disaccharides bound to the oxygen atom of post-translationally added hydroxyl groups.,similarity:Contains 1 C1q domain.,similarity:Contains 1 collagen-like domain.,subunit:C1 is a calcium-dependent trimolecular complex of C1q, R and S in the molar ration of 1:2:2. C1q subcomponent is composed of nine subunits, six of which are disulfide-linked dimers of the A and B chains, and three of which are disulfide-linked dimers of the C chain.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunohistochemistry analysis of paraffin-embedded human lung carcinoma tissue, using C1QC Antibody. The picture on the right is blocked with the synthesized peptide.

Western blot analysis of lysates from rat lung, using C1QC Antibody. The lane on the right is blocked with the synthesized peptide.

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