TNNT3 (NM_006757) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC216642L2V
- LentiORF®
Lenti ORF particles, TNNT3 (mGFP-tagged)-Human troponin T type 3 (skeletal, fast) (TNNT3), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
Product Data | |
Product Name | TNNT3 (NM_006757) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | beta-TnTF; DA2B2; TNTF |
Vector | pLenti-C-mGFP |
ACCN | NM_006757 |
ORF Size | 774 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC216642).
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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_006757.3 |
RefSeq Size | 1217 bp |
RefSeq ORF | 777 bp |
Locus ID | 7140 |
Domains | Troponin |
MW | 31 kDa |
Gene Summary | The binding of Ca(2+) to the trimeric troponin complex initiates the process of muscle contraction. Increased Ca(2+) concentrations produce a conformational change in the troponin complex that is transmitted to tropomyosin dimers situated along actin filaments. The altered conformation permits increased interaction between a myosin head and an actin filament which, ultimately, produces a muscle contraction. The troponin complex has protein subunits C, I, and T. Subunit C binds Ca(2+) and subunit I binds to actin and inhibits actin-myosin interaction. Subunit T binds the troponin complex to the tropomyosin complex and is also required for Ca(2+)-mediated activation of actomyosin ATPase activity. There are 3 different troponin T genes that encode tissue-specific isoforms of subunit T for fast skeletal-, slow skeletal-, and cardiac-muscle. This gene encodes fast skeletal troponin T protein; also known as troponin T type 3. Alternative splicing results in multiple transcript variants encoding additional distinct troponin T type 3 isoforms. A developmentally regulated switch between fetal/neonatal and adult troponin T type 3 isoforms occurs. Additional splice variants have been described but their biological validity has not been established. Mutations in this gene may cause distal arthrogryposis multiplex congenita type 2B (DA2B). [provided by RefSeq, Oct 2009] |
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