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Last updated: 2016/12/4
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HSPD1 293T Cell Transient Overexpression Lysate(Denatured)

  • Catalog # : H00003329-T02
  • Visit Frequency :
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  • Specification
  • Transfected Cell Line:
  • 293T
  • Plasmid:
  • pCMV-HSPD1 full-length
  • Host:
  • Human
  • Theoretical MW (kDa):
  • 61.1
  • Quality Control Testing:
  • Transient overexpression cell lysate was tested with Anti-HSPD1 antibody (H00003329-B01P) by Western Blots.
    SDS-PAGE Gel
    QC Testing of H00003329-T02
    HSPD1 transfected lysate.
    Western Blot
    QC Testing of H00003329-T02
    Lane 1: HSPD1 transfected lysate ( 61.10 KDa)
    Lane 2: Non-transfected lysate.
  • Storage Buffer:
  • 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
  • Storage Instruction:
  • Store at -80°C. Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Western Blot
  • Application Image
  • Western Blot
  • 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)
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