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DNAJC30 Protein (His tag)

DNAJC30 Origine: Humain Hôte: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
N° du produit ABIN7317199
  • Antigène Voir toutes DNAJC30 Protéines
    DNAJC30 (DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
    Type de proteíne
    Recombinant
    Origine
    • 1
    • 1
    Humain
    Source
    • 2
    Escherichia coli (E. coli)
    Purification/Conjugué
    Cette DNAJC30 protéine est marqué à la His tag.
    Fonction
    Recombinant Human DNAJC30 Protein (His Tag)
    Séquence
    Ser39-Gly124
    Attributs du produit
    A DNA sequence encoding the mature form of human DNAJC30 (Q96LL9) (Ser39-Gly124) was expressed with a polyhistide tag at the N-terminus.
    Pureté
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product DNAJC30 Protéine
  • Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Please refer to the printed manual for detailed information.
    Buffer
    Lyophilized from sterile PBS, pH 7.4
    Stock
    4 °C,-20 °C,-80 °C
    Stockage commentaire
    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
  • Antigène
    DNAJC30 (DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
    Autre désignation
    DNAJC30 (DNAJC30 Produits)
    Synonymes
    WBSCR18 Protein, 1300007M11Rik Protein, Wbscr18 Protein, DnaJ heat shock protein family (Hsp40) member C30 Protein, DNAJC30 Protein, Dnajc30 Protein
    Sujet

    Background: NAJC30 is a member of the DNAJ molecular chaperone homology domain-containing protein family. DNAJC30 gene is deleted in williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. DNAJC30 is expressed in brain, heart, kidney, liver, lung, spleen, stomach and testis. It contains 1 J domain. DNAJC30 is located in the Williams-Beuren syndrome (WBS) critical region. WBS results from a hemizygous deletion of several genes on chromosome 7q11.23, thought to arise as a consequence of unequal crossing over between highly homologous low-copy repeat sequences flanking the deleted region.

    Synonym: WBSCR18

    Poids moléculaire
    11.4 kDa
    UniProt
    Q96LL9
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