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AMPK alpha 1 (PRKAA1) (NM_006251) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC218572L2V
- LentiORF®
-
Lenti ORF particles, PRKAA1 (mGFP-tagged) - Human protein kinase, AMP-activated, alpha 1 catalytic subunit (PRKAA1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 11,305.00
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| Product Data | |
| Product Name | AMPK alpha 1 (PRKAA1) (NM_006251) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | AMPK; AMPKa1; AMPK alpha 1 |
| Vector | pLenti-C-mGFP |
| ACCN | NM_006251 |
| ORF Size | 1677 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC218572).
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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_006251.5, NP_006242.5 |
| RefSeq Size | 5085 bp |
| RefSeq ORF | 1680 bp |
| Locus ID | 5562 |
| Domains | pkinase, TyrKc, S_TKc |
| Protein Families | Druggable Genome, Protein Kinase |
| Protein Pathways | Adipocytokine signaling pathway, Hypertrophic cardiomyopathy (HCM), Insulin signaling pathway, mTOR signaling pathway, Regulation of autophagy |
| MW | 63.8 kDa |
| Gene Summary | The protein encoded by this gene belongs to the ser/thr protein kinase family. It is the catalytic subunit of the 5'-prime-AMP-activated protein kinase (AMPK). AMPK is a cellular energy sensor conserved in all eukaryotic cells. The kinase activity of AMPK is activated by the stimuli that increase the cellular AMP/ATP ratio. AMPK regulates the activities of a number of key metabolic enzymes through phosphorylation. It protects cells from stresses that cause ATP depletion by switching off ATP-consuming biosynthetic pathways. Alternatively spliced transcript variants encoding distinct isoforms have been observed. [provided by RefSeq, Jul 2008] |
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