HSPD1 (Human) IP-WB Antibody Pair

Catalog # H00003329-PW1

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Size:1 Set
Price: USD $ 607.00
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  • +1-909-264-1399
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Immunoprecipitation of HSPD1 transfected lysate using rabbit polyclonal anti-HSPD1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-HSPD1.

  • Specification

    Product Description

    This IP-WB antibody pair set comes with one antibody for immunoprecipitation and another to detect the precipitated protein in western blot.

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (97%); Rat (97%)

    Quality Control Testing

    Immunoprecipitation-Western Blot (IP-WB)

    Immunoprecipitation of HSPD1 transfected lysate using rabbit polyclonal anti-HSPD1 and Protein A Magnetic Bead (U0007), and immunoblotted with mouse purified polyclonal anti-HSPD1.

    Supplied Product

    Antibody pair set content:
    1. Antibody pair for IP: rabbit polyclonal anti-HSPD1 (300 ul)
    2. Antibody pair for WB: mouse purified polyclonal anti-HSPD1 (50 ug)

    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

    Immunoprecipitation-Western Blot

  • 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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