MYO7A monoclonal antibody (M01), clone 1D3
产品名称： MYO7A monoclonal antibody (M01), clone 1D3
英文名称： MYO7A monoclonal antibody (M01), clone 1D3
产品编号： H00004647-M01
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 MYO7A.
- Immunogen:
- MYO7A (NP_000251, 2118 a.a. ~ 2213 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- KQTTEPNFPEILLIAINKYGVSLIDPKTKDILTTHPFTKISNWSSGNTYFHITIGNLVRGSKLLCETSLGYKMDDLLTSYISQMLTAMSKQRGSRS
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG1 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 MYO7A is approximately 0.1ng/ml as a capture antibody.
- Protocol Download
- Entrez GeneID:
- 4647
- GeneBank Accession#:
- NM_000260
- Protein Accession#:
- NP_000251
- Gene Name:
- MYO7A
- Gene Alias:
- DFNA11,DFNB2,MYOVIIA,MYU7A,NSRD2,USH1B
- Gene Description:
- myosin VIIA
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq
- Other Designations:
- deafness, autosomal dominant 11,deafness, autosomal recessive 2,myosin VIIA (Usher syndrome 1B (autosomal recessive, severe))