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C1QC Mouse mAb (bsm-51769M)  
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50ul/1180.00元
100ul/1980.00元
大包装/询价
产品编号 bsm-51769M
英文名称 C1QC Mouse mAb
中文名称 补体C1q多肽链C单克隆抗体
别    名 C1Q-C; C1QD3; C1QG; Adib; Ciqc; C1QC_HUMAN; C1QC; C1QC_MOUSE; C1QC_RAT; complement C1q C chain; complement component 1, q subcomponent, gamma polypeptide; complement component 1, q subcomponent, C chain  补体C1q C亚基
抗体来源 Mouse
克隆类型 Monoclonal
克 隆 号 1B2
交叉反应 (predicted: Human)
产品应用 WB=1:100-1000,IHC-P=1:50-500,IF=1:50-500,ELISA=1:30-3000,IP=1:20-100
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 26kDa
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human C1QC: 101-155/245 
亚    型 IgG1, k
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 C1q, a subcomponent of the classical complement pathway, is composed of nine subunits that mediate classical complement activation and thereby play an important role in the immune response. Six of these subunits are disulfide-linked dimers of chains A and B, while three of these subunits, designated C1q-A through C1q-C, are disulfide-linked dimers of chain C. The presence of receptors for C1q on effector cells modulates its activity, which may be antibody-dependent or independent. Macrophages are the primary source of C1q, while anti-inflammatory drugs as well as cytokines differentially regulate expression of the mRNA, as well as the protein. However, its ability to modulate the interaction of platelets with collagen and immune complexes suggests C1q influences homeostasis as well as other immune activities, and perhaps thrombotic complications resulting from immune injury. Defects in C1q-A, C1q-B and C1q-C cause inactivation of the classical pathway, leading to a rare genetic disorder characterized by lupus-like symptoms.

SWISS:
P02747

Gene ID:
714

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