Bio-Connect
SDS-PAGE analysis of GTX00440-pro Human HSP60 protein (active).
SDS-PAGE analysis of GTX00440-pro Human HSP60 protein (active).
SDS-PAGE analysis of GTX00440-pro Human HSP60 protein (active).

Human HSP60 protein, His tag (active)

GTX00440-PRO
GeneTex
ApplicationsFunctional Assay
Product group Proteins / Signaling Molecules
Protein IDP10809
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    Human HSP60 protein, His tag (active)
  • Delivery Days Customer
    9
  • Application Supplier Note
    The protein has ATPase activity at the time of manufacture of 3.6 microM phosphate liberated/hr/microg protein in a 200 microl reaction at 37C (pH 7.5) in the presence of 20 microl of 1 mM ATP using a Malachite Green assay.
  • Applications
    Functional Assay
  • Certification
    Research Use Only
  • Conjugate
    Unconjugated
  • Gene ID3329
  • Target name
    HSPD1
  • Target description
    heat shock protein family D (Hsp60) member 1
  • Target synonyms
    CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13, 60 kDa heat shock protein, mitochondrial, 60 kDa chaperonin, P60 lymphocyte protein, chaperonin 60, epididymis secretory sperm binding protein, heat shock 60kDa protein 1 (chaperonin), heat shock protein 65, heat shock protein family D member 1, mitochondrial matrix protein P1, short heat shock protein 60 Hsp60s1
  • Protein IDP10809
  • Protein Name
    60 kDa heat shock protein, mitochondrial
  • Scientific Description
    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. [provided by RefSeq, Jun 2010]
  • Storage Instruction
    -20°C
  • UNSPSC
    41116100
  • Species
    Human