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Rabbit Anti-MYO3A  antibody (bs-19171R)
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-19171R
英文名称 MYO3A
中文名称 肌球蛋白3A抗体
别    名 deafness, autosomal recessive 30; DFNB30; Myo3a; MYO3A_HUMAN; Myosin IIIA; Myosin-IIIa.  
研究领域 细胞生物  免疫学  神经生物学  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 (predicted: Human,Mouse)
产品应用 IHC-P=1:100-500, IHC-F=1:100-500, ICC=1:100-500, IF=1:100-500, ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 186kDa
细胞定位 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human MYO3A: 1081-1180/1616 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 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, Jul 2008]

Function:
Probable actin-based motor with a protein kinase activity. Probably plays a role in vision and hearing.

Subcellular Location:
Cytoplasm, cytoskeleton.

Tissue Specificity:
Strongest expression in retina, retinal pigment epithelial cells, cochlea and pancreas.

DISEASE:
Deafness, autosomal recessive, 30

Similarity:
In the N-terminal section; belongs to the protein kinase superfamily.
STE Ser/Thr protein kinase family.
Contains 3 IQ domains.
Contains 1 myosin head-like domain.
Contains 1 protein kinase domain.

SWISS:
Q8NEV4

Gene ID:
53904

Database links:

Entrez Gene: 53904 Human

Omim: 606808 Human

SwissProt: Q8NEV4 Human

Unigene: 662630 Human



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