MTAP (NM_002451) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206024L4V

Lenti ORF particles, MTAP (mGFP-tagged) - Human methylthioadenosine phosphorylase (MTAP), 200ul, >10^7 TU/mL

Product Images

RC206024L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC206024L4V particle to overexpress human MTAP-mGFP fusion protein.

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  RC206024L4 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC206024L4V particle to overexpress human MTAP-mGFP fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: MTAP
• Synonyms: BDMF; c86fus; DMSFH; DMSMFH; HEL-249; LGMBF; MSAP
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-mGFP-P2A-Puro
• ACCN: NM_002451
• ORF Size: 849 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC206024).
• 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_002451.3
• RefSeq Size: 4937 bp
• RefSeq ORF: 852 bp
• Locus ID: 4507
• UniProt ID: Q13126
• Cytogenetics: 9p21.3
• Domains: Mtap_PNP
• Protein Families: Druggable Genome
• Protein Pathways: Cysteine and methionine metabolism, Metabolic pathways
• MW: 31.3 kDa
• Gene Summary: This gene encodes an enzyme that plays a major role in polyamine metabolism and is important for the salvage of both adenine and methionine. The encoded enzyme is deficient in many cancers because this gene and the tumor suppressor p16 gene are co-deleted. Multiple alternatively spliced transcript variants have been described for this gene, but their full-length natures remain unknown. [provided by RefSeq, Jul 2008]