产品属性:![]()
| 产品名称 | Collagen VI Recombinant Rabbit mAb | 规格 | 25ul、50ul、100ul |
| 抗体来源 | Rabbit | 货号 | CS-A6153 |
| 反应性 | Human,Mouse,Rat | 应用 | IHC-P,IHC-F,IF |
| 细胞定位 | 细胞浆 | 亚 型 | IgG |
| 用途 | 仅供科研研究实验 | 克隆类型 | Recombinant |
商品介绍:![]()
英文名称Collagen VI Recombinant Rabbit mAb
中文名称6型胶原重组兔单抗
别 名CO6A1_HUMAN; COL6A1; COL6A2; COL6A3; Collagen alpha 1(VI) chain; Collagen alpha 1(VI) chain precursor; Collagen alpha-1(VI) chain; Collagen type VI alpha 1; Collagen type VI alpha 2; Collagen type VI alpha 3; Collagen VI alpha 1 polypeptide; Collagen VI alpha 2 polypeptide; Collagen VI alpha 3 polypeptide; CollagenVI; Human mRNA for collagen VI alpha 1 C terminal globular domain; OPLL; PP3610.
抗体来源Rabbit
克隆类型Recombinant
克 隆 号4D10
交叉反应Human,Mouse,Rat
产品应用WB=1:1000-5000,IHC-P=1:200-800,IHC-F=1:200-800,IF=1:200-800
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量106 kDa
检测分子量
细胞定位细胞浆
性 状Liquid
免 疫 原A synthesized peptide derived from human Collagen VI: 15-250
亚 型IgG
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 °C 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.
PubMedPubMed
Collagen VI Recombinant Rabbit mAb产品介绍
The collagens are a superfamily of proteins that play a role in maintaining the integrity of various tissues. Collagens are extracellular matrix proteins and have a triple-helical domain as their common structural element. Collagen VI is a major structural component of microfibrils. The basic structural unit of collagen VI is a heterotrimer of the alpha1(VI), alpha2(VI), and alpha3(VI) chains. The alpha2(VI) and alpha3(VI) chains are encoded by the COL6A2 and COL6A3 genes, respectively. The protein encoded by this gene is the alpha 1 subunit of type VI collagen (alpha1(VI) chain). Mutations in the genes that code for the collagen VI subunits result in the autosomal dominant disorder, Bethlem myopathy. [provided by RefSeq, Jul 2008]
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