ROR2 monoclonal antibody (M03), clone 2A10
產品名稱： ROR2 monoclonal antibody (M03), clone 2A10
英文名稱： ROR2 monoclonal antibody (M03), clone 2A10
產品編號： H00004920-M03
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 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