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Last updated: 2017/10/15

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HSPD1 rabbit monoclonal antibody

  • Catalog # : H00003329-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human HSPD1 peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human HSPD1 is used for rabbit immunization.
    Customer or Abnova will decide on the preferred peptide sequence.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Purification:
  • Protein A
  • Isotype:
  • IgG
  • Quality Control Testing:
  • Antibody reactive against human HSPD1 peptide by ELISA and mammalian transfected lysate by Western Blot.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • 1. Customer may provide cell or tissue lysate for antibody screening.
    2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.
  • Library Construction:
  • Non-fusion antibody library from rabbit spleen (ARM Technology).
  • Expression:
  • Overexpression vector and transfection into 293H cell line.
  • Deliverable:
  • Up to three rabbit IgG clones of 1 mg each will be delivered to customer.
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Transfected lysate)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 3329
  • GeneBank Accession#:
  • HSPD1
  • 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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