DFNA5 抗体
Quick Overview for DFNA5 抗体 (ABIN7113358)
抗原
See all DFNA5 抗体适用
宿主
克隆类型
标记
应用范围
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纯化方法
- Immunogen affinity purified
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纯度
- ≥95 % as determined by SDS-PAGE
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免疫原
- deafness, autosomal dominant 5
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亚型
- IgG
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anti-Deafness, Autosomal Dominant 5 (DFNA5) (C-Term) antibody
DFNA5 适用: 人, 小鼠 WB, ELISA, IHC, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 111-200) antibodyDFNA5 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 1E10 unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 342-391) antibodyDFNA5 适用: 人, Cow, 犬, 豚鼠, 猴 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (C-Term) antibodyDFNA5 适用: 人, 大鼠, Cow, 犬, 豚鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 59-87), (N-Term) antibodyDFNA5 适用: 人 WB, IHC (p), FACS 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 21-120) antibodyDFNA5 适用: 大鼠, 小鼠 WB, ELISA, IF (cc), IF (p), IHC (p), ICC, IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (Internal Region) antibodyDFNA5 适用: 人, 大鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 1-496) antibodyDFNA5 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) (AA 1-295) antibodyDFNA5 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Deafness, Autosomal Dominant 5 (DFNA5) antibody (Biotin)DFNA5 适用: 人 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal Biotin
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应用备注
- WB: 1:500 - 1:2000, IHC: 1:50 - 1:200
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3 ,
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- -20°C for 12 months (Avoid repeated freeze / thaw cycles.)
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有效期
- 12 months
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- DFNA5 (Deafness, Autosomal Dominant 5 (DFNA5))
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别名
- DFNA5
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背景
- Synonyms:deafness, autosomal dominant 5, DFNA5, ICERE 1, ICERE1 Background:Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene.
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分子量
- Refer to figures
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基因ID
- 1687
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UniProt
- O60443
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途径
- Sensory Perception of Sound
抗原
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