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货号： bs-18242R-RBITC 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-18242R-RBITC
- 英文名称
- Anti-LHFPL5/RBITC
- 中文名称
- 罗丹明（RBITC）标记的脂肪瘤高迁移率融合蛋白样蛋白5抗体
- 别 名
- Lhfpl5; LHPL5_HUMAN; Lipoma HMGIC fusion partner like 5; Lipoma HMGIC fusion partner-like 5 protein.
- 规格价格
- 100ul/2980元购买 大包装/询价
- 说 明 书
- 100ul
- 研究领域
- 细胞生物 免疫学 神经生物学
- 抗体来源
- Rabbit
- 克隆类型
- Polyclonal
- 交叉反应
- Human, Mouse, Rat, Cow, Horse, Sheep,
- 产品应用
- ICC=1:50-200 IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
- 分 子 量
- 24kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human LHFPL5
- 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.
- 产品介绍
- background:
This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis. [provided by RefSeq, Jul 2008]
Function:
May function in hair bundle morphogenesis.
Subcellular Location:
Membrane.
DISEASE:
Defects in LHFPL5 are a cause of deafness autosomal recessive type 67 (DFNB67) [MIM:610265]. DFNB67 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.
Similarity:
Belongs to the LHFP family.
Database links:Entrez Gene: 222662Human
Entrez Gene: 328789Mouse
Entrez Gene: 294303Rat
Omim: 609427Human
SwissProt: Q8TAF8Human
SwissProt: Q4KL25Mouse
SwissProt: Q5PPI7Rat
Unigene: 367947Human
Unigene: 284760Mouse
Unigene: 161732Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.