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货号： bs-16312R 基本售价： 1380.0 元 规格： 100ul
- 规格：100ul
- 价格：1380.00元
- 规格：200ul
- 价格：2200.00元
产品信息
- 产品编号
- bs-16312R
- 英文名称
- GRHL2/DFNA28
- 中文名称
- 耳聋常染色体显性遗传蛋白28抗体
- 别 名
- BOM; Brother of mammalian grainyhead; Deafness autosomal dominant 28; DFNA28; FLJ11172; FLJ13782; Grainyhead like 2 (Drosophila); Grainyhead like 2; Grainyhead like protein 2 homolog; Grainyhead-like protein 2 homolog; GRHL 2; GRHL2; GRHL2_HUMAN; MGC149294; MGC149295; RGD1561191; TFCP2L3; Transcription factor CP2 like 3; Transcription factor CP2-like 3.
- 规格价格
- 100ul/1380元购买 200ul/2200元购买 大包装/询价
- 说 明 书
- 100ul 200ul
- 研究领域
- 细胞生物 发育生物学 神经生物学 生长因子和激素 表观遗传学
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Chicken, Pig, Cow, Rabbit, Sheep,
- 产品应用
- ELISA=1:500-1000 IHC-P=1:400-800 IHC-F=1:400-800 ICC=1:100-500 IF=1:100-500 （石蜡切片需做抗原修复）
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 71kDa
- 细胞定位
- 细胞核
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human GRHL2/DFNA28:551-625/625
- 亚 型
- IgG
- 纯化方法
- affinity purified by Protein A
- 储 存 液
- 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
- 保存条件
- Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
- PubMed
- PubMed
- 产品介绍
- background:
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).[provided by RefSeq, Mar 2009]
Function:
May function as a transcription factor.
Subcellular Location:
Nucleus.
Tissue Specificity:
Highly expressed in placenta, prostate, brain and kidney. Lower-level expression in a variety of epithelial tissues such as thymus, kidney, lung, salivary gland, mammary gland and digestive tract. Expressed in the cochlear.
DISEASE:
Defects in GRHL2 are the cause of deafness autosomal dominant type 28 (DFNA28) [MIM:608641]. DFNA28 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. DFNA28 is characterized by mild to moderate hearing loss across most frequencies that progressed to severe loss in the higher frequencies by the fifth decade. Age at onset varied, with the earliest case documented at 7 years of age.
Similarity:
Belongs to the grh/CP2 family. Grainyhead subfamily.
SWISS:
Q6ISB3
Gene ID:
79977
Database links:Entrez Gene: 79977Human
Entrez Gene: 252973Mouse
Entrez Gene: 299979Rat
Omim: 608576Human
SwissProt: Q6ISB3Human
SwissProt: Q8K5C0Mouse
Unigene: 661088Human
Unigene: 244612Mouse
Unigene: 99340Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.