ROR2 monoclonal antibody (M03), clone 2A10
产品名称： ROR2 monoclonal antibody (M03), clone 2A10
英文名称： ROR2 monoclonal antibody (M03), clone 2A10
产品编号： H00004920-M03
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 ROR2.
- Immunogen:
- ROR2 (NP_004551, 34 a.a. ~ 143 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- EVEVLDPNDPLGPLDGQDGPIPTLKGYFLNFLEPVNNITIVQGQTAILHCKVAGNPPPNVRWLKNDAPVVQEPRRIIIRKTEYGSRLRIQDLDTTDTGYYQCVATNGMKT
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG2a Kappa
- Storage Buffer:
- In 1x PBS, pH 7.2
- Storage Instruction:
- Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
- Quality Control Testing:
- Antibody Reactive Against Recombinant Protein.
- MSDS:
Download
- Applications
- Sandwich ELISA (Recombinant protein)
- Detection limit for recombinant GST tagged ROR2 is approximately 10ng/ml as a capture antibody.
- Protocol Download
- Application Image
- Sandwich ELISA (Recombinant protein)
- ELISA
- Entrez GeneID:
- 4920
- GeneBank Accession#:
- NM_004560
- Protein Accession#:
- NP_004551
- Gene Name:
- ROR2
- Gene Alias:
- BDB,BDB1,MGC163394,NTRKR2
- Gene Description:
- receptor tyrosine kinase-like orphan receptor 2
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene is a receptor protein tyrosine kinase and type I transmembrane protein that belongs to the ROR subfamily of cell surface receptors. The protein may be involved in the early formation of the chondrocytes and may be required for cartilage and growth plate development. Mutations in this gene can cause brachydactyly type B, a skeletal disorder characterized by hypoplasia/aplasia of distal phalanges and nails. In addition, mutations in this gene can cause the autosomal recessive form of Robinow syndrome, which is characterized by skeletal dysplasia with generalized limb bone shortening, segmental defects of the spine, brachydactyly, and a dysmorphic facial appearance. [provided by RefSeq
- Other Designations:
- OTTHUMP00000021634,OTTHUMP00000063680,neurotrophic tyrosine kinase receptor-related 2,tyrosine-protein kinase transmembrane receptor ROR2