HSPD1 (Human) Matched Antibody Pair

Catalog # H00003329-AP21

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Price

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Quantity

Size:1 Set
Price: USD $ 607.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human HSPD1.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (97%); Rat (97%)

    Quality Control Testing

    Standard curve using recombinant protein ( H00003329-P01 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 3 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-HSPD1 (100 ug)
    2. Detection antibody: mouse purified polyclonal anti-HSPD1 (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — HSPD1

    Entrez GeneID

    3329

    Gene Name

    HSPD1

    Gene Alias

    CPN60, GROEL, HLD4, HSP60, HSP65, HuCHA60, SPG13

    Gene Description

    heat shock 60kDa protein 1 (chaperonin)

    Omim ID

    118190 605280

    Gene Ontology

    Hyperlink

    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)

  • Interactome
  • Pathway
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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