ADAMTS3 monoclonal antibody (M08A), clone 1D6
产品名称: ADAMTS3 monoclonal antibody (M08A), clone 1D6
英文名称: ADAMTS3 monoclonal antibody (M08A), clone 1D6
产品编号: H00009508-M08A
产品价格: null
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围:
亚诺法生技股份有限公司(Abnova)
- 联系人 :
- 地址 : 台湾台北市内湖区洲子街 108 号 9 楼
- 邮编 : 11493
- 所在区域 : 台湾
- 电话 : +886-920**1152 点击查看
- 传真 : 点击查看
- 邮箱 : sales@abnova.com.tw
- Specification
- Product Description:
- Mouse monoclonal antibody raised against a partial recombinant ADAMTS3.
- Immunogen:
- ADAMTS3 (NP_055058.1, 1048 a.a. ~ 1128 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- ESCSKRSSTLPPPYLLEAAETHDDVISNPSDLPRSLVMPTSLVPYHSETPAKKMSLSSISSVGGPNAYAAFRPNSKPDGAN
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG2a Kappa
- Storage Buffer:
- In ascites fluid
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
Western Blot detection against Immunogen (34.65 KDa) .
- Applications
- Western Blot (Cell lysate)
- ADAMTS3 monoclonal antibody (M08A), clone 1D6. Western Blot analysis of ADAMTS3 expression in Jurkat.
- Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Entrez GeneID:
- 9508
- GeneBank Accession#:
- NM_014243
- Protein Accession#:
- NP_055058.1
- Gene Name:
- ADAMTS3
- Gene Alias:
- ADAMTS-4,KIAA0366
- Gene Description:
- ADAM metallopeptidase with thrombospondin type 1 motif, 3
- Omim ID:
- 605011
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of the family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members of this family differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The protein encoded by this gene is the major procollagen II N-propeptidase. A deficiency of this protein may be responsible for dermatosparaxis, a genetic defect of connective tissues. [provided by RefSeq
- Other Designations:
- a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 3,zinc metalloendopeptidase
- Related Disease