Product Browser

Last updated: 2014/10/27

Product Compare

Product Compare Cancel Click this icon to add products to compare list. Select up to 10 products.

Quick Order (Tutorial)

Input Catalog #,
place order here!
Catalog # :
  • Where to buy
  • Choose your location

HSPD1 (Human) ELISA Kit

  • Catalog # : KA1843
  • Visit Frequency :
  • Countries :
  • Specification
  • Product Description:
  • HSPD1 (Human) ELISA Kit is a sandwich enzyme immunoassay for the quantitative measurement of human HSPD1.
  • Limit of Detection:
  • 2 ng/mL
  • Reactivity:
  • Human
  • Quality Control Testing:
  • Standard Curve

    QC Testing of KA1843
    The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.
  • Storage Instruction:
  • Store components of the kit at 4°C or -20°C as described in the protocol.
  • Suitable Sample:
  • Cell Lysate, Plasma, Serum, Tissue Lysate
  • Sample Volume:
  • 50 uL
  • Label:
  • Biotin-conjugate
  • Detection Method:
  • Colorimetric
  • Intra-Assay:
  • 4.8%
  • Inter-Assay:
  • 7.2%
  • Spiking Recovery:
  • 97%
  • Regulation Status:
  • For research use only (RUO)
  • Applications
  • Quantification
  • Application Image
  • Quantification
  • Gene Information
  • Entrez GeneID:
  • 3329
  • Gene Name:
  • HSPD1
  • Gene Alias:
  • CPN60,GROEL,HLD4,HSP60,HSP65,HuCHA60,SPG13
  • Gene Description:
  • heat shock 60kDa protein 1 (chaperonin)
  • Gene Summary:
  • 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. Two pseudogenes, both located on chromosome 8, 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
  • Other Designations:
  • P60 lymphocyte protein,chaperonin,heat shock 60kD protein 1 (chaperonin),heat shock protein 65,mitochondrial heat shock 60kD protein 1 variant 1,mitochondrial matrix protein P1,short heat shock protein 60 Hsp60s1,spastic paraplegia 13 (autosomal dominant)
  • RSS
  • YouTube
  • Linkedin
  • Facebook