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- 抗原 See all Myosin VIIA (MYO7A) 抗体
- Myosin VIIA (MYO7A)
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抗原表位
- AA 850-1150
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Myosin VIIA antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- MIARRLHQRL RAEYLWRLEA EKMRLAEEEK LRKEMSAKKA KEEAERKHQE RLAQLAREDA ERELKEKEAA RRKKELLEQM ERARHEPVNH SDMVDKMFGF LGTSGGLPGQ EGQAPSGFED LERGRREMVE EDLDAALPLP DEDEEDLSEY KFAKFAATYF QGTTTHSYTR RPLKQPLLYH DDEGDQLAAL AVWITILRFM GDLPEPKYHT AMSDGSEKIP VMTKIYETLG KKTYKRELQA LQGEGEAQLP EGQKKSSVRH KLVHLTLKKK SKLTEEVTKR LHDGESTVQG NSMLEDRPTS N
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 850-1150 of human MYO7A (NP_000251.3).
- 亚型
- IgG
- Top Product
- Discover our top product MYO7A Primary Antibody
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anti-Myosin VIIA (MYO7A) antibody
MYO7A 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myosin VIIA (MYO7A) (AA 838-968) antibodyMYO7A 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin VIIA (MYO7A) (AA 851-950) antibodyMYO7A 适用: 人, 小鼠 ELISA, IF (cc), IF (p), IHC (fro), IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Myosin VIIA (MYO7A) (AA 2118-2213) antibodyMYO7A 适用: 人 ELISA, WB 宿主: 小鼠 Polyclonal unconjugated
anti-Myosin VIIA (MYO7A) (AA 2118-2213) antibodyMYO7A 适用: 人 ELISA 宿主: 小鼠 Monoclonal 1D3 unconjugated
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- 应用备注
- WB,1:500 - 1:2000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- Myosin VIIA (MYO7A)
- 别名
- MYO7A (MYO7A 产品)
- 背景
- 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.,MYO7A,DFNA11,DFNB2,MYOVIIA,MYU7A,NSRD2,USH1B,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,MYO7A
- 分子量
- 138 kDa/240 kDa/249 kDa/250 kDa/254 kDa
- 基因ID
- 4647
- UniProt
- Q13402
- 途径
- Sensory Perception of Sound
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