CDH23 抗体
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- 抗原 See all CDH23 抗体
- CDH23 (Cadherin 23 (CDH23))
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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 CDH23 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Antigen affinity purification
- 免疫原
- Fusion protein of Human CDH23
- 亚型
- IgG
- Top Product
- Discover our top product CDH23 Primary Antibody
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- 应用备注
- ELISA:1:2000-1:5000, WB:1:500-1:2000, IHC:1:100-1:300,
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- 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,-80 °C
- 储存方法
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- 抗原
- CDH23 (Cadherin 23 (CDH23))
- 别名
- CDH23 (CDH23 产品)
- 别名
- 4930542A03Rik antibody, USH1D antibody, ahl antibody, ahl1 antibody, bob antibody, bus antibody, mdfw antibody, nmf112 antibody, nmf181 antibody, nmf252 antibody, sals antibody, v antibody, CDHR23 antibody, W antibody, cadherin 23 (otocadherin) antibody, cadherin related 23 antibody, cadherin-related 23 antibody, Cdh23 antibody, CDH23 antibody
- 背景
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Background: This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.
Aliases: CDH23 antibody, KIAA1774 antibody, KIAA1812 antibody, UNQ1894/PRO4340Cadherin-23 antibody, Otocadherin antibody
- UniProt
- Q9H251
- 途径
- Sensory Perception of Sound
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