TCF4 (1-507, His-Tag) Human Protein
CAT#: AR51425PU-N
Recombinant human TCF4 protein
Size: 50 ug
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CNY 17930.00
货期*
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规格
Specifications
Product Data | |
Species | Human |
Expression Host | E. coli |
Expression cDNA Clone or AA Sequence |
|
Tag | His-Tag |
Predicted MW | 56.6 kDa (530aa) |
Concentration | 0.5mg/ml (determined by Bradford assay) |
Purity | > 85% by SDS-PAGE |
Buffer | Liquid in. 20mM Tris-HCl buffer (pH 8.0) containing 10% glycerol 0.1M NaCl |
Preparation | Liquid purified protein |
Applications | SDS-PAGE |
Protein Description | Recombinant human TCF4 protein, fused to His-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography. |
Storage | Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80C. Avoid repeated freezing and thawing cycles. |
Stability | Shelf life: one year from despatch. |
Reference Data | |
RefSeq | NP_001230165.1 |
Locus ID | 6925 |
UniProt ID | P15884 |
Cytogenetics | 18q21.2 |
Synonyms | Transcription factor 4, bHLHb19, E2-2, ITF-2, ITF2, PTHS, SEF-2, SEF2, SEF2-1, SEF2-1A, SEF2-1B, TCF-4 |
Summary | This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016] |
Protein Families | Druggable Genome, ES Cell Differentiation/IPS, Transcription Factors |
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