anti-BBS5 antibody

Key features and details

  • 产品描述: Rabbit Polyclonal antibody recognizes BBS5
  • 反应物种: Hu
  • 应用: WB
  • 宿主: Rabbit
  • 克隆: Polyclonal
  • 同位型: IgG
  • 靶点名称: BBS5
  • 抗原物种: Human
  • 抗原: KLH-conjugated synthetic peptide corresponding to aa. 108-141 (Center) of Human BBS5.
  • Brand:
CAT.NO. : ARG55859
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Product Details
概述
产品描述Rabbit Polyclonal antibody recognizes BBS5
反应物种Hu
应用WB
宿主Rabbit
克隆Polyclonal
同位型IgG
靶点名称BBS5
抗原物种Human
抗原KLH-conjugated synthetic peptide corresponding to aa. 108-141 (Center) of Human BBS5.
偶联标记Un-conjugated
別名Bardet-Biedl syndrome 5 protein
应用说明
应用建议
应用推荐稀释比
WB1:1000
应用说明* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
阳性对照K562
属性
形式Liquid
纯化Purification with Protein A and immunogen peptide.
缓冲液PBS and 0.09% (W/V) Sodium azide
抗菌剂0.09% (W/V) Sodium azide
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: 129880 Human BBS5

Swiss-port # Q8N3I7 Human Bardet-Biedl syndrome 5 protein

基因名称BBS5
全名Bardet-Biedl syndrome 5
背景介绍This gene encodes a protein that has been directly linked to Bardet-Biedl syndrome. The primary features of this syndrome include retinal dystrophy, obesity, polydactyly, renal abnormalities and learning disabilities. Experimentation in non-human eukaryotes suggests that this gene is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized. [provided by RefSeq, Jul 2008]
生物功能The BBSome complex is thought to function as a coat complex required for sorting of specific membrane proteins to the primary cilia. The BBSome complex is required for ciliogenesis but is dispensable for centriolar satellite function. This ciliogenic function is mediated in part by the Rab8 GDP/GTP exchange factor, which localizes to the basal body and contacts the BBSome. Rab8(GTP) enters the primary cilium and promotes extension of the ciliary membrane. Firstly the BBSome associates with the ciliary membrane and binds to RAB3IP/Rabin8, the guanosyl exchange factor (GEF) for Rab8 and then the Rab8-GTP localizes to the cilium and promotes docking and fusion of carrier vesicles to the base of the ciliary membrane. The BBSome complex, together with the LTZL1, controls SMO ciliary trafficking and contributes to the sonic hedgehog (SHH) pathway regulation. Required for BBSome complex ciliary localization but not for the proper complex assembly. [UniProt]
细胞定位Cell projection, cilium membrane. Cytoplasm. Cytoplasm, cytoskeleton, cilium basal body Cytoplasm, cytoskeleton, microtubule organizing center, centrosome, centriolar satellite. Note=Localizes to basal bodies
预测分子量39 kDa
检测图片 (1)
  • ARG55859 anti-BBS5 antibody WB image

    Western blot: 35 µg of K562 cell lysate stained with ARG55859 anti-BBS5 antibody at 1:1000 dilution.

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