POU4F3 (NM_002700) Human Recombinant Protein
CAT#: TP761435
Purified recombinant protein of Human POU class 4 homeobox 3 (POU4F3), full length, with N-terminal GST and C-terminal HIS tag, expressed in E. coli, 50ug
View other "POU4F3" proteins (2)
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Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
A DNA sequence encoding human full-length POU4F3
|
Tag | N-GST and C-His |
Predicted MW | 64.9 kDa |
Concentration | >0.05 µg/µL as determined by microplate BCA method |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Buffer | 25 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1% sarkosyl, 10% glycerol |
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. |
Reference Data | |
RefSeq | NP_002691 |
Locus ID | 5459 |
UniProt ID | Q15319 |
Refseq Size | 1182 |
Cytogenetics | 5q32 |
Refseq ORF | 1014 |
Synonyms | BRN3C; DFNA15; DFNA42; DFNA52 |
Summary | This gene encodes a member of the POU-domain family of transcription factors. POU-domain proteins have been observed to play important roles in control of cell identity in several systems. This protein is found in the retina and may play a role in determining or maintaining the identities of a small subset of visual system neurons. Defects in this gene are the cause of non-syndromic sensorineural deafness autosomal dominant type 15. [provided by RefSeq, Mar 2009] |
Protein Families | Transcription Factors |
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