Cyclin T1 (CCNT1) (NM_001240) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC217377L4V
- LentiORF®
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Lenti ORF particles, CCNT1 (mGFP-tagged)-Human cyclin T1 (CCNT1), 200ul, >10^7 TU/mL. Note: ORF is codon optimized
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CNY 15,295.00
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Specifications
Product Data | |
Product Name | Cyclin T1 (CCNT1) (NM_001240) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CCNT; CYCT1; HIVE1 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001240 |
ORF Size | 2178 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC217377).
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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_001240.3, NP_001231.2 |
RefSeq Size | 6788 bp |
RefSeq ORF | 2181 bp |
Locus ID | 904 |
Protein Families | Druggable Genome, Transcription Factors |
MW | 80.7 kDa |
Gene Summary | This gene encodes a member of the highly conserved cyclin C subfamily. The encoded protein tightly associates with cyclin-dependent kinase 9, and is a major subunit of positive transcription elongation factor b (p-TEFb). In humans, there are multiple forms of positive transcription elongation factor b, which may include one of several different cyclins along with cyclin-dependent kinase 9. The complex containing the encoded cyclin and cyclin-dependent kinase 9 acts as a cofactor of human immunodeficiency virus type 1 (HIV-1) Tat protein, and is both necessary and sufficient for full activation of viral transcription. This cyclin and its kinase partner are also involved in triggering transcript elongation through phosphorylation of the carboxy-terminal domain of the largest RNA polymerase II subunit. Overexpression of this gene is implicated in tumor growth. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2013] |
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