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Aco1 (NM_007386) Mouse Tagged ORF Clone Lentiviral Particle
CAT＃: MR211074L4V
- LentiORF®
-
Lenti ORF particles, Aco1 (GFP-tagged) - Mouse aconitase 1 (Aco1), 200ul, >10^7 TU/mL
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CNY 15,485.00
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Specifications
| Product Data | |
| Product Name | Aco1 (NM_007386) Mouse Tagged ORF Clone Lentiviral Particle |
| Synonyms | Aco-1; Irebp; Irp1 |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_007386 |
| ORF Size | 2667 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(MR211074).
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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_007386.2 |
| RefSeq Size | 4319 bp |
| RefSeq ORF | 2670 bp |
| Locus ID | 11428 |
| Gene Summary | This gene encodes a member of the aconitase/IPM isomerase protein family. The encoded protein has been identified as a moonlighting protein based on its ability to perform mechanistically distinct functions. Depending on iron levels in the cytosol, the encoded protein can function as either an aconitase enzyme or as an mRNA binding protein. When cellular iron levels are high, the encoded protein functions as an aconitase, an essential enzyme in the TCA cycle that catalyzes the conversion of citrate to isocitrate. When cellular iron levels are low, the encoded protein regulates iron uptake and utilization by binding to iron-responsive elements in the untranslated regions of mRNAs for genes involved in iron metabolism. Disruption of this gene is associated with pulmonary hypertension and polycythemia. [provided by RefSeq, Jan 2014] |
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