CDH23 抗体
Quick Overview for CDH23 抗体 (ABIN7112149)
抗原
See all CDH23 抗体适用
宿主
克隆类型
标记
应用范围
-
-
原理
- CDH23 antibody
-
纯化方法
- Immunogen affinity purified
-
纯度
- ≥95 % as determined by SDS-PAGE
-
免疫原
- cadherin-like 23
-
亚型
- IgG
-
-
anti-Cadherin 23 (CDH23) antibody
CDH23 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (AA 34-236) antibodyCDH23 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (C-Term) antibodyCDH23 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (AA 29-114) antibodyCDH23 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (N-Term) antibodyCDH23 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (N-Term) antibodyCDH23 适用: 人, 小鼠, 大鼠 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (Internal Region) antibodyVerified CDH23 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (AA 61-110) antibodyCDH23 适用: 人, 小鼠, 大鼠 ELISA, IHC, IF, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Cadherin 23 (CDH23) (N-Term) antibodyCDH23 适用: 人, 小鼠, 大鼠 IF, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- WB: 1:500 - 1:2000, IHC: 1:100 - 1:200
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
缓冲液
- PBS with 0.02 % sodium azide and 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.
-
注意事项
- Avoid repeated freeze / thaw cycles.
-
储存条件
- -20 °C
-
储存方法
- -20°C for 12 months
-
有效期
- 12 months
-
-
- CDH23 (Cadherin 23 (CDH23))
-
别名
- CDH23
-
背景
-
Synonyms: Cadherin-23|Otocadherin|CDH23|KIAA1774|KIAA1812
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. Upregulation of this gene may also be associated with breast cancer. Alternative splice variants encoding different isoforms have been described.
-
分子量
- 59 kDa
-
基因ID
- 64072
-
UniProt
- Q9H251
-
途径
- Sensory Perception of Sound
抗原
-
