GSDME (NM_004403) Human Recombinant Protein
CAT#: TP310515
Recombinant protein of human deafness, autosomal dominant 5 (DFNA5), transcript variant 1, 20 µg
Size: 100 ug 1 mg
Product Images
Specifications
| Product Data | |
| Species | Human |
| Expression Host | HEK293T |
| Expression cDNA Clone or AA Sequence | >RC210515 protein sequence Red=Cloning site Green=Tags(s) MFAKATRNFLREVDADGDLIAVSNLNDSDKLQLLSLVTKKKRFWCWQRPKYQFLSLTLGDVLIEDQFPSP VVVESDFVKYEGKFANHVSGTLETALGKVKLNLGGSSRVESQSSFGTLRKQEVDLQQLIRDSAERTINLR NPVLQQVLEGRNEVLCVLTQKITTMQKCVISEHMQVEEKCGGIVGIQTKTVQVSATEDGNVTKDSNVVLE IPAATTIAYGVIELYVKLDGLFEFCLLRGKQGGFENKKRIDSVYLDHLVFREFAFIDMPDAAHGISSQDG PLSVLKQATLLLERNFHPFAELPEPQQTALSDIFQAVVFDDELLMVLEPVCDDLVSGLSPTVAVLGELKP RQQQDLVAFLQLVGCSLQGGCPGPEDAGSKQLFMTAYFLVSALAEMPDSAAALLGTCCKLQIIPTLCHLL RALSDDGVSDLEDPTLTPLKDTERFGIVQRLFASADISLERLKSSVKAVILKDSKVFPLLLCITLNGLCA LGREHS TRTRPLEQKLISEEDLAANDILDYKDDDDKV |
| Tag | C-Myc/DDK |
| Predicted MW | 54.4 kDa |
| Concentration | >0.1 µg/µL as determined by microplate BCA method |
| Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
| Buffer | 25 mM Tris-HCl, 100 mM glycine, pH 7.3, 10% glycerol |
| Preparation | Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps. |
| 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_004394 |
| Locus ID | 1687 |
| UniProt ID | O60443, A0A024RA58 |
| Cytogenetics | 7p15.3 |
| Refseq Size | 2521 |
| Refseq ORF | 1488 |
| Synonyms | DFNA5; ICERE-1 |
| Summary | Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008] |
| Protein Families | Druggable Genome |
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Resources
Recombinant Protein Resources |
Other Versions
| SKU | Description | Size | |
|---|---|---|---|
| LC418010 | DFNA5 HEK293T cell transient overexpression lysate (as WB positive control) | 134,00 EUR | |
| LC426790 | DFNA5 HEK293T cell transient overexpression lysate (as WB positive control) | 134,00 EUR | |
| LY418010 | Transient overexpression lysate of deafness, autosomal dominant 5 (DFNA5), transcript variant 1 | 436,00 EUR | |
| LY426790 | Transient overexpression lysate of deafness, autosomal dominant 5 (DFNA5), transcript variant 2 | 436,00 EUR | |
| PH310515 | DFNA5 MS Standard C13 and N15-labeled recombinant protein (NP_004394) | 3 255,00 EUR |