PDE1C (NM_005020) Human Recombinant Protein
CAT#: TP760557
Purified recombinant protein of Human phosphodiesterase 1C, calmodulin-dependent 70kDa (PDE1C), transcript variant 4, with N-terminal HIS tag, expressed in E.Coli, 50ug
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CNY 2,040.00
货期*
现货
规格
Cited in 1 publication. |
经常一起买 (1)
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length PDE1C
|
Tag | N-His |
Predicted MW | 72 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 50 mM Tris-HCl, pH 8.0, 8 M urea |
Note | For testing in cell culture applications, please filter before use. Note that you may experience some loss of protein during the filtration process. |
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. |
Bioactivity | Enzyme activity (PMID: 29860631) |
Reference Data | |
RefSeq | NP_005011 |
Locus ID | 5137 |
UniProt ID | Q14123 |
Refseq Size | 2694 |
Cytogenetics | 7p14.3 |
Refseq ORF | 1902 |
Synonyms | cam-PDE 1C; DFNA74; hCam-3; Hcam3 |
Summary | This gene encodes an enzyme that belongs to the 3'5'-cyclic nucleotide phosphodiesterase family. Members of this family catalyze hydrolysis of the cyclic nucleotides, cyclic adenosine monophosphate and cyclic guanosine monophosphate, to the corresponding nucleoside 5'-monophosphates. The enzyme encoded by this gene regulates proliferation and migration of vascular smooth muscle cells, and neointimal hyperplasia. This enzyme also plays a role in pathological vascular remodeling by regulating the stability of growth factor receptors, such as PDGF-receptor-beta. [provided by RefSeq, Jul 2016] |
Protein Families | Druggable Genome |
Protein Pathways | Calcium signaling pathway, Olfactory transduction, Progesterone-mediated oocyte maturation, Purine metabolism |
Citations (1)
The use of this Proteins has been cited in the following citations: |
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A dominant variant in the PDE1C gene is associated with nonsyndromic hearing loss
,Wang, L;Feng, Y;Yan, D;Qin, L;Grati, M;Mittal, R;Li, T;Sundhari, AK;Liu, Y;Chapagain, P;Blanton, SH;Liao, S;Liu, X;,
Hum. Genet.
,PubMed ID 29860631
[PDE1C]
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