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ACSM2A (NM_001010845) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC220982L4V
- LentiORF®
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Lenti ORF particles, ACSM2A (mGFP-tagged) - Human acyl-CoA synthetase medium-chain family member 2A (ACSM2A), nuclear gene encoding mitochondrial protein, 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50
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USD 365.00
Specifications
| Product Data | |
| Type | Human Tagged ORF Clone Lentiviral Particle |
| Tag | mGFP |
| Symbol | ACSM2A |
| Synonyms | A-923A4.1; ACSM2 |
| Mammalian Cell Selection | Puromycin |
| Vector | pLenti-C-mGFP-P2A-Puro |
| ACCN | NM_001010845 |
| ORF Size | 1731 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC220982).
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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_001010845.1, NP_001010845.1 |
| RefSeq Size | 2322 bp |
| RefSeq ORF | 1734 bp |
| Locus ID | 123876 |
| Cytogenetics | 16p12.3 |
| Protein Pathways | Butanoate metabolism, Metabolic pathways |
| MW | 64 kDa |
| Gene Summary | This gene encodes a mitochondrial acyl-coenzyme A synthetase that is specific for medium chain fatty acids. These enzymes catalyze fatty acid activation, the first step of fatty acid metabolism, through the transfer of acyl-CoA. These enzymes also participate in the glycine conjugation pathway in the detoxification of xenobiotics such as benzoate and ibuprofen. Expression levels of this gene in the kidney may be correlated with kidney function. This gene and its paralog ACSM2B (Gene ID: 348158), both present on chromosome 16, likely arose from a chromosomal duplication event. [provided by RefSeq, May 2017] |
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