ADAMTS3 monoclonal antibody (M08A), clone 1D6
產品名稱: ADAMTS3 monoclonal antibody (M08A), clone 1D6
英文名稱: ADAMTS3 monoclonal antibody (M08A), clone 1D6
產品編號: H00009508-M08A
產品價格: null
產品產地: 臺灣
品牌商標: Abnova
更新時間: null
使用范圍:
亞諾法生技股份有限公司(Abnova)
- 聯系人 :
- 地址 : 臺灣臺北市內湖區洲子街 108 號 9 樓
- 郵編 : 11493
- 所在區域 : 臺灣
- 電話 : +886-920**1152 點擊查看
- 傳真 : 點擊查看
- 郵箱 : 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
