CDH23 polyclonal antibody (A01)
产品名称： CDH23 polyclonal antibody (A01)
英文名称： CDH23 polyclonal antibody (A01)
产品编号： H00064072-A01
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 polyclonal antibody raised against a partial recombinant CDH23.
- Immunogen:
- CDH23 (NP_071407, 29 a.a. ~ 114 a.a) partial recombinant protein with GST tag.
- Sequence:
- PFFTNHFFDTYLLISEDTPVGSSVTQLLAQDMDNDPLVFGVSGEEASRFFAVEPDTGVVWLRQPLDRETKSEFTVEFSVSDHQGVI
- Host:
- Mouse
- Reactivity:
- Human
- Storage Buffer:
- 50 % glycerol
- 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 (35.57 KDa) .
- MSDS:
Download
- Publication Reference
- 1.
- Cadherin-23 Mediates Heterotypic Cell-Cell Adhesion between Breast Cancer Epithelial Cells and Fibroblasts.
Apostolopoulou M, Ligon L.PLoS One. 2012;7(3):e33289. Epub 2012 Mar 7.
- Application Image
- Western Blot (Recombinant protein)
- ELISA
- Entrez GeneID:
- 64072
- GeneBank Accession#:
- NM_022124
- Protein Accession#:
- NP_071407
- Gene Name:
- CDH23
- Gene Alias:
- DFNB12,DKFZp434P2350,FLJ00233,FLJ36499,KIAA1774,KIAA1812,MGC102761,USH1D
- Gene Description:
- cadherin-like 23
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is a large, single-pass transmembrane protein composed of an extracellular domain containing 27 repeats that show significant homology to the cadherin ectodomain. Expressed in the neurosensory epithelium, the protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Two alternative splice variants have been identified that encode different isoforms. Additional variants have been observed but their full-length nature has not been determined. [provided by RefSeq
- Other Designations:
- OTTHUMP00000044780,cadherin 23,cadherin related 23,cadherin-23,otocadherin