CEP57 ?rabbit polyclonal antibody
應(yīng)用:Western Blot: 1/500 - 1/2000. ELISA: 1/40000. ?
產(chǎn)品名:CEP57 ? rabbit Polyclonal Antibody
貨號(hào):ATA26668?
種類(Category)
Primary antibodies
宿主(Host)
Rabbit
反應(yīng)種屬(Species specificity)
Human
應(yīng)用實(shí)驗(yàn)(Tested applications)
WB,ELISA
克隆性(Clonality)
Polyclonal
偶連物(Conjugation)
Unconjugated
免疫原(Immunogen)
The antiserum was produced against synthesized peptide derived from human CEP57. AA range:241-290
狀態(tài)(Form)
Liquid
存放條件(Storage)
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 4 °C for frequent use. Store at -20 to -80 °C for twelve months from the date of receipt.
純化方式(Purity)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
產(chǎn)品背景:centrosomal protein 57(CEP57) Homo sapiens This gene encodes a cytoplasmic protein called Translokin. This protein localizes to the centrosome and has a function in microtubular stabilization. The N-terminal half of this protein is required for its centrosome localization and for its multimerization, and the C-terminal half is required for nucleating, bundling and anchoring microtubules to the centrosomes. This protein specifically interacts with fibroblast growth factor 2 (FGF2), sorting nexin 6, Ran-binding protein M and the kinesins KIF3A and KIF3B, and thus mediates the nuclear translocation and mitogenic activity of the FGF2. It also interacts with cyclin D1 and controls nucleocytoplasmic distribution of the cyclin D1 in quiescent cells. This protein is crucial for maintaining correct chromosomal number during cell division. Mutations in this gene cause mosaic variegated aneuploidy syndrome, a rare autosomal recessive disorder. Multiple?
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