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Troponin T1 (TNNT1) (NM_001126133) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC225325L4V
- LentiORF®
-
Lenti ORF particles, TNNT1 (mGFP-tagged) - Human troponin T type 1 (skeletal, slow) (TNNT1), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
| Product Data | |
| Product Name | Troponin T1 (TNNT1) (NM_001126133) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | ANM; NEM5; STNT; TNT; TNTS |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001126133 |
| ORF Size | 753 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC225325).
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| OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
| OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
| Reference Data | |
| RefSeq | NM_001126133.1 |
| RefSeq ORF | 756 bp |
| Locus ID | 7138 |
| Protein Families | Druggable Genome |
| MW | 29.9 kDa |
| Gene Summary | 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. [provided by RefSeq, Jul 2008] |
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