Recombinant Human HSPD1 / HSP60 Protein (His & GST tag)

  • Catalog number
    PKSH031150-50µg
  • Price
    Please ask
  • Size
    50µg
  • Synonym
    CPN60;GROEL;HLD4;HSP-60;HSP60;HSP65;HuCHA60;SPG13
  • Activity
    NA
  • Sequence
    Leu 2-Phe 573
  • Fusion tag
    N-His & GST
  • Accession
    NP_955472.1
  • Expressed Host
    E. coli
  • Shipping
    In general, recombinant proteins are provided as lyophilized powder which are shipped at ambient temperature.Bulk packages of recombinant proteins are provided as frozen liquid. They are shipped out with blue ice unless customers require otherwise.
  • Purity
    >90 % as determined by SDS-PAGE
  • Endotoxin
    Please contact us for more information.
  • Stability and Storage
    Samples are stable for up to twelve months from date of receipt at -70℃.Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
  • Mol Mass
    88.7 kDa
  • AP Mol Mass
    52-65 kDa
  • Formulation
    Lyophilized from sterile PBS, pH 7.4
  • Background
    HSPD1, also known as HSP60, is a member of the chaperonin family. HSPD1 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. It may also prevent misfolding and promote the refolding and proper assembly of unfolded polypeptides generated under stress conditions in the mitochondrial matrix. HSPD1 gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13.Defects in HSPD1 are a cause of spastic paraplegia autosomal dominant type 13 (SPG13). Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Defects in HSPD1 are the cause of leukodystrophy hypomyelinating type 4 (HLD4); also called mitochondrial HSP60 chaperonopathy or MitCHAP-60 disease. HLD4 is a severe autosomal recessive hypomyelinating leukodystrophy. HSPD1 is cinically characterized by infantile-onset rotary nystagmus, progressive spastic paraplegia, neurologic regression, motor impairment, profound mental retardation. Death usually occurrs within the first two decades of life.Immune Checkpoint   Immunotherapy   Cancer Immunotherapy   Targeted Therapy
  • Conjugation
    histidine
  • Properties
    Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.
  • Source
    Recombinants or rec. proteins
  • Group
    recombinants
  • Gene target
    HSPD1   HSP60   Protein   His   GST   tag  
  • Gene symbol
    HSPD1, MGST3, HSPD1P1, HSPD1P14, HSPD1P20, HSPD1P8, HSPD1P4, HSPD1P16, HSPD1P21, HSPD1P17
  • Short name
    Recombinant HSPD1 / HSP60 Protein (His & GST tag)
  • Technique
    Recombinant, E. coli recombinant proteins are genetic recombinations in Escherichia coli, supplied as white sterile powder lyopillized. Elabscience advises they will be reconstituted in a buffer soluion or culture medium for cell culture. Tags
  • Label
    His
  • Species
    Human, Humans
  • Alternative name
    Rec. H. sapiens heat shock 60kDa protein 1 (chaperonin) / HSP60 Protein (histidine & GST detection labelled)
  • Alternative technique
    rec
  • Alternative to gene target
    heat shock 60kDa protein 1 (chaperonin), CPN60 and GROEL and HLD4 and HSP-60 and HSP60 and HSP65 and HuCHA60 and SPG13, HSPD1 and IDBG-77925 and ENSG00000144381 and 3329, chaperone binding, Extracellular, Hspd1 and IDBG-155162 and ENSMUSG00000025980 and 102641967,15510, BT.89909 and IDBG-642936 and ENSBTAG00000012586 and 511913
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1
  • Synonyms gene
  • Synonyms gene name
    • heat shock 60kD protein 1 (chaperonin)
    • spastic paraplegia 13 (autosomal dominant)
    • heat shock 60kDa protein 1 (chaperonin)
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1991-07-19
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • Chaperonins
  • VEGA ID
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1 pseudogene 1
  • Synonyms gene name
    • heat shock 60kDa protein 1 (chaperonin) pseudogene 1
  • Synonyms
  • Locus
  • Discovery year
    2008-09-22
  • Entrez gene record
  • VEGA ID
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1 pseudogene 20
  • Synonyms gene name
    • heat shock 60kDa protein 1 (chaperonin) pseudogene 20
  • Synonyms
  • Locus
  • Discovery year
    2010-06-25
  • Entrez gene record
  • RefSeq identity
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1 pseudogene 8
  • Synonyms gene name
    • heat shock 60kDa protein 1 (chaperonin) pseudogene 8
  • Synonyms
  • Locus
  • Discovery year
    2008-09-22
  • Entrez gene record
  • VEGA ID
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1 pseudogene 4
  • Synonyms gene name
    • heat shock 60kDa protein 1 (chaperonin) pseudogene 4
  • Synonyms
  • Locus
  • Discovery year
    2008-09-22
  • Entrez gene record
  • VEGA ID
Gene info
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    heat shock protein family D (Hsp60) member 1 pseudogene 17
  • Synonyms gene name
    • heat shock 60kDa protein 1 (chaperonin) pseudogene 17
  • Synonyms
  • Locus
  • Discovery year
    2008-09-22
  • Entrez gene record
  • RefSeq identity
MeSH Data
  • Name
  • Concept
    Scope note: The initial culturing of cells derived directly from fresh TISSUES.
  • Tree numbers
    • E01.370.225.500.223.500
    • E05.200.500.265.500
    • E05.242.223.500
    • E05.481.500.249.500
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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