USH1G 抗体
The 兔 多克隆 anti-USH1G antibody (ABIN7120659) specifically detects USH1G in ELISA 和 IP.
The antibody is reactive with 人 samples.
产品编号 ABIN7120659
发货至:
中国
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Contact Info
Our Local Distributor
中国
北京 101111
北京 101111
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Beijing Economic Technological Development Area
Room 801-803
Quick Overview for USH1G 抗体 (ABIN7120659)
抗原
See all USH1G 抗体
USH1G
(Usher Syndrome 1G (Autosomal Recessive) (USH1G))
适用
人
宿主
兔
克隆类型
多克隆
标记
This USH1G antibody is un-conjugated
应用范围
ELISA, Immunoprecipitation (IP)
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原理
- USH1G antibody
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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
- Usher syndrome 1G(autosomal recessive)
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亚型
- IgG
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应用备注
- IP: 1:200-1:2000
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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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注意事项
- Avoid repeated freeze / thaw cycles.
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储存条件
- -20 °C
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储存方法
- -20°C for 12 months
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有效期
- 12 months
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- USH1G (Usher Syndrome 1G (Autosomal Recessive) (USH1G))
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别名
- USH1G
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背景
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Synonyms: pre-mRNA splicing regulator USH1G|Scaffold protein containing ankyrin repeats and SAM domain|Usher syndrome type-1G protein|USH1G|SANS
Background: Required for normal development and maintenance of cochlear hair cell bundles. Anchoring/scaffolding protein that is a part of the functional network formed by USH1C, USH1G, CDH23 and MYO7A that mediates mechanotransduction in cochlear hair cells. Required for normal hearing.
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分子量
- 52 kDa
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基因ID
- 124590
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UniProt
- Q495M9
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途径
- Sensory Perception of Sound
抗原
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