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DNAJC30 Protein (His tag)

DNAJC30 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 95 % as determined by reducing SDS-PAGE.
Catalog No. ABIN7317199
  • Target See all DNAJC30 Proteins
    DNAJC30 (DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
    Protein Type
    Recombinant
    Origin
    • 1
    • 1
    Human
    Source
    • 2
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This DNAJC30 protein is labelled with His tag.
    Purpose
    Recombinant Human DNAJC30 Protein (His Tag)
    Sequence
    Ser39-Gly124
    Characteristics
    A DNA sequence encoding the mature form of human DNAJC30 (Q96LL9) (Ser39-Gly124) was expressed with a polyhistide tag at the N-terminus.
    Purity
    > 95 % as determined by reducing SDS-PAGE.
    Top Product
    Discover our top product DNAJC30 Protein
  • 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
    Storage
    4 °C,-20 °C,-80 °C
    Storage Comment
    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.
  • Target
    DNAJC30 (DnaJ (Hsp40) Homolog, Subfamily C, Member 30 (DNAJC30))
    Alternative Name
    DNAJC30 (DNAJC30 Products)
    Synonyms
    WBSCR18 Protein, 1300007M11Rik Protein, Wbscr18 Protein, DnaJ heat shock protein family (Hsp40) member C30 Protein, DNAJC30 Protein, Dnajc30 Protein
    Background

    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

    Molecular Weight
    11.4 kDa
    UniProt
    Q96LL9
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