HSP60 Antibody Pair

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    • Catalog Number
      H00003329-AP21
    • Availability
      Product Discontinued

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HSP60 Antibody Pair Summary

Description
Quality control test: Standard curve using recombinant protein (H00003329-P01) as an analyte. This antibody pair set comes with matched antibody pair to detect and quantify protein level of human HSPD1.

  • Capture antibody: rabbit MaxPab affinity purified polyclonal anti-HSPD1 (100 ug)
  • Detection antibody: mouse purified polyclonal anti-HSPD1 (20 ug)
  • Marker
    Mitochondria Marker
    Standard Curve Range
    3 ng/ml to 100 ng/ml
    Assay Type
    Sandwich ELISA
    Clonality
    Monoclonal
    Gene
    HSPD1

    Applications/Dilutions

    Dilutions
    • Sandwich ELISA 3 ng/ml - 100 ng/ml

    Packaging, Storage & Formulations

    Storage
    Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
    Buffer
    1x PBS, pH 7.4

    Notes

    This product is produced by and distributed for Abnova, a company based in Taiwan.

    Alternate Names for HSP60 Antibody Pair

    • 60 kDa chaperonin
    • Chaperonin 60
    • cpn60
    • GROEL
    • heat shock 60kD protein 1 (chaperonin)
    • heat shock 60kDa protein 1 (chaperonin)
    • Heat shock protein 60
    • heat shock protein 65
    • HLD4
    • HSP60
    • HSP-60
    • HSP60SPG13
    • HSP65
    • HSPD1
    • HuCHA60
    • Mitochondrial matrix protein P1,60 kDa heat shock protein, mitochondrial
    • P60 lymphocyte protein
    • short heat shock protein 60 Hsp60s1
    • spastic paraplegia 13 (autosomal dominant)
    • SPG13

    Background

    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]

    Limitations

    This product is for research use only and is not approved for use in humans or in clinical diagnosis. Antibody Pairs are guaranteed for 6 months from date of receipt.

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    Bioinformatics

    Gene Symbol HSPD1