MYO3A monoclonal antibody (M08A), clone 8H2
產品名稱： MYO3A monoclonal antibody (M08A), clone 8H2
英文名稱： MYO3A monoclonal antibody (M08A), clone 8H2
產品編號： H00053904-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 MYO3A.
- Immunogen:
- MYO3A (NP_059129, 1400 a.a. ~ 1490 a.a) partial recombinant protein with GST tag. MW of the GST tag alone is 26 KDa.
- Sequence:
- HEEINNIKKKDNKDSKATSEREACGLAIFSKQISKLSEEYFILQKKLNEMILSQQLKSLYLGVSHHKPINRRVSSQQCLSGVCKGEEPKIL
- Host:
- Mouse
- Reactivity:
- Human
- Isotype:
- IgG2b
- 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 (35.64 KDa) .
- MSDS:
Download
- Applications
- Western Blot (Cell lysate)
- MYO3A monoclonal antibody (M08A), clone 8H2 Western Blot analysis of MYO3A expression in Hela NE ( Cat # L013V3 ).
- Protocol Download
- Western Blot (Recombinant protein)
- Protocol Download
- Entrez GeneID:
- 53904
- GeneBank Accession#:
- NM_017433
- Protein Accession#:
- NP_059129
- Gene Name:
- MYO3A
- Gene Alias:
- DFNB30
- Gene Description:
- myosin IIIA
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The protein encoded by this gene belongs to the myosin superfamily. Myosins are actin-dependent motor proteins and are categorized into conventional myosins (class II) and unconventional myosins (classes I and III through XV) based on their variable C-terminal cargo-binding domains. Class III myosins, such as this one, have a kinase domain N-terminal to the conserved N-terminal motor domains and are expressed in photoreceptors. The protein encoded by this gene plays an important role in hearing in humans. Three different recessive, loss of function mutations in the encoded protein have been shown to cause nonsyndromic progressive hearing loss. Expression of this gene is highly restricted, with the strongest expression in retina and cochlea. [provided by RefSeq
- Other Designations:
- OTTHUMP00000019339