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CEP104 Polyclonal antibody

CEP104 Polyclonal Antibody for WB, ELISA
Cat No. 31847-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, ELISA

KIAA0562, Centrosomal protein of 104 kDa, Centrosomal Protein 104kDa, Centrosomal Protein 104

缓冲液配方:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive WB detected inHeLa cells, HepG2 cells, K-562 cells, MOLT-4 cells, SK-BR-3 cells, hTERT-RPE1 cells

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:2000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

31847-1-AP targets CEP104 in WB, ELISA applications and shows reactivity with human samples.

经测试应用 WB, ELISA Application Description
经测试反应性 human
免疫原

CatNo: Ag35662

Product name: Recombinant human KIAA0562 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-200 aa of NM_014704.3

Sequence: MPHKIGFVVVSSSGHEDGFSARELMIHAPTVSGWRSPRFCQFPQEIVLQMVERCRIRKLQLLAHQYMISSKIEFYISESLPEYFAPYQAERFRRLGYVSLCDNEKTGCKARELKSVYVDAVGQFLKLIFHQNHVNKYNIYNQVALVAINIIGDPADFSDESNTASREKLIDHYLGHNSEDPALEGTYARKSDYISPLDDL

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 KIAA0562
别名 KIAA0562, Centrosomal protein of 104 kDa, Centrosomal Protein 104kDa, Centrosomal Protein 104
计算分子量104kDa,925aa
观测分子量70 kDa
GenBank蛋白编号NM_014704.3
基因名称 KIAA0562
Gene ID (NCBI) 9731
RRIDAB_3742485
偶联类型 Unconjugated
形式Liquid
纯化方式Antigen affinity Purification
UNIPROT IDO60308
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

KIAA0562, also known as CEP104 (centrosomal protein 104), is a gene encoding a centrosomal protein that is essential for ciliogenesis and the structural integrity of the cilium tip. During ciliogenesis, CEP104 is translocated from the distal tip of the centriole to the elongated cilium tip. CEP104 is expressed in a variety of cell types, including tissues such as testis and kidney. Mutations in its gene are associated with the autosomal recessive disorder Joubert syndrome, which is characterized by distinctive mid-hindbrain and cerebellar malformations, actinic dyskinesia, irregular breathing, developmental delay, and ataxia. In studies, inhibitors of CEP104 such as Cytochalasin D and Vismodegib have been used to investigate their specific role in cellular function.

实验方案

Product Specific Protocols
WB protocol for CEP104 antibody 31847-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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