HSPD1 293T Cell Transient Overexpression Lysate(Denatured)

Catalog # H00003329-T01

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Size:100 uL
Price: USD $ 247.00
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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
SDS-PAGE Gel
QC Test

SDS-PAGE Gel

HSPD1 transfected lysate.

Western Blot
QC Test

Western Blot

Lane 1: HSPD1 transfected lysate ( 63.14 KDa)
Lane 2: Non-transfected lysate.

  • Specification

    Transfected Cell Line

    293T

    Plasmid

    pCMV-HSPD1 full-length

    Host

    Human

    Theoretical MW (kDa)

    63.14

    Interspecies Antigen Sequence

    Mouse (98); Rat (98)

    Quality Control Testing

    Transient overexpression cell lysate was tested with Anti-HSPD1 antibody (H00003329-B01) by Western Blots.

    SDS-PAGE Gel

    HSPD1 transfected lysate.

    Western Blot

    Lane 1: HSPD1 transfected lysate ( 63.14 KDa)
    Lane 2: Non-transfected lysate.

    Storage Buffer

    1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)

    Storage Instruction

    Store at -80°C. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot

  • Gene Info — HSPD1

    Entrez GeneID

    3329

    GeneBank Accession#

    NM_002156.4

    Protein Accession#

    NP_002147.2

    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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