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货号： bs-19352R-PE-Cy5.5 基本售价： 2980.0 元 规格： 100ul
产品信息
- 产品编号
- bs-19352R-PE-Cy5.5
- 英文名称
- Anti-NRN1L/PE-Cy5.5
- 中文名称
- PE-Cy5.5标记的转化神经突起蛋白1样蛋白抗体
- 别 名
- MRCC2446; Neuritin-like protein; Nrn1l; NRN1L_HUMAN; UNQ2446/PRO5725.
- 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,
- 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
- 18kDa
- 性 状
- Lyophilized or Liquid
- 浓 度
- 1mg/ml
- 免 疫 原
- KLH conjugated synthetic peptide derived from human NRN1L
- 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:
NRN1L is a 165 amino acid membrane protein that belongs to the neuritin family. The gene that encodes NRN1L consists of approximately 1,495 bases and maps to human chromosome 16q22.1. Encoding over 900 genes and consisting of approximately 90 million base pairs, chromosome 16 makes up nearly 3% of the human genome and is associated with a variety of genetic disorders. The GAN gene is located on chromosome 16 and, when mutated, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. Alterations in the CREB gene and NOD2 gene, both of which are located on chromosome 16, results in Rubinstein-Taybi syndrome and Crohns disease, respectively.
Subcellular Location:
Cell membrane.
Similarity:
Belongs to the neuritin family.
Database links:Entrez Gene: 123904Human
SwissProt: Q496H8Human
Unigene: 435464Human
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.