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Product Name
Human DNAJC30 (His Tag) recombinant protein
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Description
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.
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Protein name
DnaJ homolog subfamily C member 30
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Protein short names
WILLIAMS-BEUREN SYNDROME CRITICAL REGION 18; WILLIAMS-BEUREN SYNDROME CHROMOSOMAL REGION 18 PROTEIN HOMOLOG; WILLIAMS-BEUREN SYNDROME CHROMOSOME REGION 18 HOMOLOG; DNAJC30; MEMBER 30; WILLIAMS BEUREN SYNDROME CHROMOSOME REGION 18; DNAJ HOMOLOG SUBFAMILY C MEMBER 30; SUBFAMILY C; 1300007M11RIK; WBSCR18; DNAJ (HSP40) HOMOLOG; WILLIAMS-BEUREN SYNDROME CHROMOSOMAL REGION 18 PROTEIN
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Uniprot ID
Q96LL9
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Gene Name
DNAJC30; WBSCR18
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Source/Expression Host
E. coli
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Expression Plasmid/cDNA
A DNA sequence encoding the mature form of human DNAJC30 (Q96LL9) (Ser39-Gly124) was expressed with a polyhistide tag at the N-terminus.
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Protein Species
Human
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Molecular weight
The recombinant human DNAJC30 consists of 101 amino acids and predicts a molecular mass of 11.4 KDa. It migrates as an approximately 14 KDa band in SDS-PAGE under reducing conditions.
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Purity
> 95 % as determined by SDS-PAGE
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Validations
Human DNAJC30 Protein (His Tag) SDS-PAGE
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