HSPD1 monoclonal antibody, clone 14

Catalog # MAB9977

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Price

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Quantity

Size:100 ug
Price: USD $ 329.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Cell lysate)
Application

Western Blot (Cell lysate)

Western blot analysis of HepG2 whole cell lystae with HSPD1 monoclonal antibody, clone 14 (Cat # MAB9977) at 1:1000 dilution.

  • Specification

    Product Description

    Mouse monoclonal antibody raised against full length recombinant HSPD1.

    Immunogen

    Recombinant protein corresponding to full length human HSPD1.

    Host

    Mouse

    Reactivity

    Human

    Specificity

    It can expression in HepG2 whole cell lysate.

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG1

    Recommend Usage

    Western blot (1:1000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In Citrate-Tris-HCl buffer, pH 7.0 (0.02% Proclin 300)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Cell lysate)

    Western blot analysis of HepG2 whole cell lystae with HSPD1 monoclonal antibody, clone 14 (Cat # MAB9977) at 1:1000 dilution.

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — HSPD1

    Entrez GeneID

    3329

    Protein Accession#

    P10809

    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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