DNAJC30 Protein (His Tag)

18.04.2013

Sino Biological Inc. liefert DNAJC30 Protein (His Tag) mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über DNAJC30 Protein (His Tag) lesen Sie bitte: http://www.sinobiological.com/DNAJC30-Protein-Antibody-a-5858.html

Produkt-Information von DNAJC30 Protein

Synonym	DNAJC30, WBSCR18
Protein Construction	A DNA sequence encoding the mature form of human DNAJC30 (Q96LL9) (Ser39-Gly124) was expressed with a polyhistide tag at the N-terminus.
Source	Human
Expression Host	E.coli

QC Testing von DNAJC30 Protein

Purity	> 95 % as determined by SDS-PAGE	SDS-PAGE: DNAJC30 protein
Endotoxin	Please contact us for more information.
Stability	Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal	His
Molecular Mass	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.
Formulation	Lyophilized from sterile PBS, pH 7.4. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA. Please contact us for any concerns or special requirements.

Usage Guide von DNAJC30 Protein

Storage	Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution	A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

Beschreibung von DNAJC30 Protein

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.

References

Hillier L W. et al., 2003, Nature. 424: 157-64.
Ota T. et al., 2004, Nat Genet. 36: 40-5.
Merla G. et al., 2002, Hum Genet. 110: 429-38.

DNAJC30 related areas, pathways, and other information