DHH (NM_021044) Human Recombinant Protein
CAT#: TP760621
Purified recombinant protein of Human desert hedgehog (DHH), with N-terminal HIS tag, expressed in E.Coli, 50ug
Other products for "DHH"
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length DHH
|
Tag | N-His |
Predicted MW | 41.3 kDa |
Concentration | >50 ug/mL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50mM Tris,8M Urea,pH8.0. |
Storage | Store at -80°C. |
Stability | Stable for 12 months from the date of receipt of the product under proper storage and handling conditions. Avoid repeated freeze-thaw cycles. |
Reference Data | |
RefSeq | NP_066382 |
Locus ID | 50846 |
UniProt ID | O43323 |
Cytogenetics | 12q13.12 |
Refseq Size | 1971 |
Refseq ORF | 1188 |
Synonyms | GDXYM; HHG-3; SRXY7 |
Summary | This gene encodes a member of the hedgehog family. The hedgehog gene family encodes signaling molecules that play an important role in regulating morphogenesis. This protein is predicted to be made as a precursor that is autocatalytically cleaved; the N-terminal portion is soluble and contains the signalling activity while the C-terminal portion is involved in precursor processing. More importantly, the C-terminal product covalently attaches a cholesterol moiety to the N-terminal product, restricting the N-terminal product to the cell surface and preventing it from freely diffusing throughout the organism. Defects in this protein have been associated with partial gonadal dysgenesis (PGD) accompanied by minifascicular polyneuropathy. This protein may be involved in both male gonadal differentiation and perineurial development. [provided by RefSeq, May 2010] |
Protein Families | Druggable Genome, ES Cell Differentiation/IPS, Protease |
Protein Pathways | Hedgehog signaling pathway |
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