Thermo Fisher Scientific HSP60 Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

1:500-1:2,000

-

Immunohistochemistry (Paraffin) (IHC (P))

1:50-1:200

-

Immunocytochemistry (ICC/IF)

1:50-1:100

-

Immunoprecipitation (IP)

1:50-1:200

-

Product Specifications

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 27-240 of human Hsp60 if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:HSP60,uniProtId:P10809-1,ncbiNodeId:9606,antigenRange:27-240,antigenLength:573,antigenImageFileName:PA5-87538_HSP60_P10809-1_Rabbit.svg,antigenImageFileNamePDP:PA5-87538_HSP60_P10809-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

1.79 mg/mL

Storage conditions

-20° C, Avoid Freeze/Thaw Cycles

Shipping conditions

Wet ice

RRID

AB_2804235

Product Specific Information

Immunogen sequence: AKDVKFGADA RALMLQGVDL LADAVAVTMG PKGRTVIIEQ SWGSPKVTKD GVTVAKSIDL KDKYKNIGAK LVQDVANNTN EEAGDGTTTA TVLARSIAKE GFEKISKGAN PVEIRRGVML AVDAVIAELK KQSKPVTTPE EIAQVATISA NGDKEIGNII SDAMKKVGRK GVITVKDGKT LNDELEIIEG MKFDRGYISP YFINTSKGQK CEFQ; Positive Samples: HeLa, Jurkat, K-562, Mouse kidney, Mouse liver, Mouse thymus, Rat heart; Cellular Location: Mitochondrion matrix

Target Information

This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.