anti-Wnt1 antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes Wnt1
  • 反应物种: Hu
  • 应用: WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: Wnt1
  • 抗原物种: Human
  • 抗原: Synthetic peptide of Human Wnt1. (NLLTDSKSLQLVLEPSLQLLSRKQRRLIRQ)
  • Brand:
CAT.NO. : ARG58132
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes Wnt1
反应物种Hu
应用WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称Wnt1
抗原物种Human
抗原Synthetic peptide of Human Wnt1. (NLLTDSKSLQLVLEPSLQLLSRKQRRLIRQ)
偶联标记Un-conjugated
別名Proto-oncogene Wnt-1; Proto-oncogene Int-1 homolog; INT1; BMND16; OI15
应用说明
应用建议
应用推荐稀释比
WB0.1 - 0.5 µg/ml
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
属性
形式Liquid
纯化Affinity purification with immunogen.
缓冲液PBS, 0.025% Sodium azide and 2.5% BSA.
抗菌剂0.025% Sodium azide
稳定剂2.5% BSA
浓度0.5 mg/ml
存放说明For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
注意事项For laboratory research only, not for drug, diagnostic or other use.
生物信息
数据库连接

GeneID: 7471 Human WNT1

Swiss-port # P04628 Human Proto-oncogene Wnt-1

基因名称WNT1
全名wingless-type MMTV integration site family, member 1
背景介绍The WNT gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene is a member of the WNT gene family. It is very conserved in evolution, and the protein encoded by this gene is known to be 98% identical to the mouse Wnt1 protein at the amino acid level. The studies in mouse indicate that the Wnt1 protein functions in the induction of the mesencephalon and cerebellum. This gene was originally considered as a candidate gene for Joubert syndrome, an autosomal recessive disorder with cerebellar hypoplasia as a leading feature. However, further studies suggested that the gene mutations might not have a significant role in Joubert syndrome. This gene is clustered with another family member, WNT10B, in the chromosome 12q13 region. [provided by RefSeq, Jul 2008]
生物功能Ligand for members of the frizzled family of seven transmembrane receptors. In some developmental processes, is also a ligand for the coreceptor RYK, thus triggering Wnt signaling. Probable developmental protein. May be a signaling molecule important in CNS development. Is likely to signal over only few cell diameters. Has a role in osteoblast function and bone development. [UniProt]
预测分子量41 kDa
翻译后修饰Palmitoleylation is required for efficient binding to frizzled receptors. Palmitoleylation is necessary for proper trafficking to cell surface (Probable). Depalmitoleylated by NOTUM, leading to inhibit Wnt signaling pathway (By similarity). [UniProt]
检测图片 (1)
  • ARG58132 anti-Wnt1 antibody WB image

    Western blot: COLO320 cell lysate stained with ARG58132 anti-Wnt1 antibody.

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