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Anti-ATRNL1抗体
描述:

Anti-ATRNL1抗体ATRNL1 is a 1,379 amino acid single-pass type I membrane protein that may play a role in melanocortin signaling pathways that regulate energy homeostasis.

  • 产品型号:
  • 厂商性质:生产厂家
  • 更新时间:2015-10-26
  • 访问量:58
产品介绍/ PRODUCT PRESENTATION

产品编号 yb-11504R
英文名称 Anti-ATRNL1抗体
中文名称 ATRNL1蛋白抗体
别    名 ATRN1_HUMAN; ATRNL1; Attractin-like protein 1; KIAA0534.
Anti-ATRNL1抗体 
说 明 书 0.2ml  
研究领域 细胞生物  神经生物学  信号转导  细胞膜受体  G蛋白偶联受体  G蛋白信号  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, Rabbit, Sheep, 
产品应用 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 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 147kDa
细胞定位 细胞膜 
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human ATRNL1
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:
ATRNL1 is a 1,379 amino acid single-pass type I membrane protein that may play a role in melanocortin signaling pathways that regulate energy homeostasis. The ATRNL1 protein contains a C-type lectin domain, a CUB domain, two EGF-like domains, six Kelch repeats, two laminin EGF-like domains and five PSI domains. ATRNL1 interacts with MC4-R in several regions known to be important in the regulation of energy homeostasis by melanocortins, such as the paraventricular nucleus of hypothalamus and the dorsal motor nucleus of the vagus. The ATRNL1 gene is conserved in dog, cow, mouse, rat, chicken, zebrafish and C. elegans, exists as two alternatively spliced isoforms and maps to human chromosome 10q25.3. Strong evidence of linkage to late-onset Alzheimer disease (LOAD) is linked to chromosome 10, which implicates a wide region and at least one disease-susceptibility locus.

Function:
May play a role in melanocortin signaling pathways that regulate energy homeostasis.

Subunit:
Interacts with MC4R

Subcellular Location:
Membrane; Single-pass type I membrane protein

Similarity:
Contains 1 C-type lectin domain.
Contains 1 CUB domain.
Contains 2 EGF-like domains.
Contains 6 Kelch repeats.
Contains 2 laminin EGF-like domains.
Contains 5 PSI domains.

Database links:
UniProtKB/Swiss-Prot: Q5VV63.2

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

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