| Brand Name: | Flarebio |
|---|---|
| Application: | Laboratories |
| Appearance: | powder |
| Purity: | >90% |
| Grade Standard: | Reagent Grade |
| Place of Origin: | China (Mainland) |
Quick Details
Specifications
| Product Name: | Recombinant Human Troponin T, slow skeletal muscle(TNNT1) |
| Product Type : | Recombinant Protein |
| Size : | 1mg |
| Uniprot NO. : | |
| Storage : | Store at -20℃, for extended storage, conserve at -20℃ or -80℃. |
| Storage Buffer : | Tris-based buffer,50% glycerol |
| Code : |
CSB-YP024015HU >> Yeast CSB-EP024015HU >> E.coli CSB-BP024015HU >> Baculovirus CSB-MP024015HU >> Mammalian cell |
| Species : | Homo sapiens (Human) |
| Purity : | >90% |
| Sequence : | MSDTEEQEYE EEQPEEEAAE EEEEAPEEPE PVAEPEEERP KPSRPVVPPL IPPKIPEGER VDFDDIHRKR MEKDLLELQT LIDVHFEQRK KEEEELVALK ERIERRRSER AEQQRFRTEK ERERQAKLAE EKMRKEEEEA KKRAEDDAKK KKVLSNMGAH FGGYLVKAEQ KRGKRQTGRE MKVRILSERK KPLDIDYMGE EQLRARSAWL PPSQPSCPAR EKAQELSDWI HQLESEKFDL MAKLKQQKYE INVLYNRISH AQKFRKGAGK GRVGGRWK |
| Gene Names : | Name:TNNT1 Synonyms:TNT |
| Protein Names : | Recommended name: Troponin T, slow skeletal muscle Short name= TnTs Alternative name(s): Slow skeletal muscle troponin T Short name= sTnT |
| Expression Region : | 1-278 |
| Notes : | Repeated freezing and thawing is not recommended. Store working aliquots at 4℃ for up to one week. |
| Product Info : | His tagged |
| Protein Description : | Full length protein |
| Target details : | This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene. |
| HGNC : | |
| RGD : | |
| MGI : | |
| BIOWWW : | |
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