ASS1 (NM_054012) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC201130L3V

Lenti ORF particles, ASS1 (Myc-DDK tagged) - Human argininosuccinate synthase 1 (ASS1), transcript variant 2, 200ul, >10^7 TU/mL

Product Images

RC201130L3 was used to prepare Lentiviral particles using TR30037 packaging kit. HEK293T cells were transduced with RC201130L3V particle to overexpress human ASS1-Myc-DDK fusion protein.

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: ASS1
• Synonyms: ASS; CTLN1
• Mammalian Cell Selection: Puromycin
• Vector: pLenti-C-Myc-DDK-P2A-Puro
• ACCN: NM_054012
• ORF Size: 1236 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC201130).
• 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_054012.3
• RefSeq Size: 1801 bp
• RefSeq ORF: 1239 bp
• Locus ID: 445
• UniProt ID: P00966
• Cytogenetics: 9q34.11
• Domains: Arginosuc_synth
• Protein Families: Druggable Genome
• Protein Pathways: Alanine, aspartate and glutamate metabolism, Arginine and proline metabolism, Metabolic pathways
• MW: 46.5 kDa
• Gene Summary: The protein encoded by this gene catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 copies of this gene including the pseudogenes scattered across the human genome, among which the one located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. Mutations in the chromosome 9 copy of this gene cause citrullinemia. Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Aug 2012]