GAK (NM_005255) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC223572L1V

Lenti ORF particles, GAK (Myc-DDK tagged) - Human cyclin G associated kinase (GAK), 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: Myc-DDK
• Symbol: GAK
• Synonyms: DNAJ26; DNAJC26
• Vector: pLenti-C-Myc-DDK
• ACCN: NM_005255
• ORF Size: 3933 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC223572).
• 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_005255.1, NP_005246.1
• RefSeq Size: 4331 bp
• RefSeq ORF: 3936 bp
• Locus ID: 2580
• Cytogenetics: 4p16.3
• Domains: pkinase, TyrKc, DnaJ, S_TKc
• Protein Families: Druggable Genome, Protein Kinase
• MW: 143 kDa
• Gene Summary: 'In all eukaryotes, the cell cycle is governed by cyclin-dependent protein kinases (CDKs), whose activities are regulated by cyclins and CDK inhibitors in a diverse array of mechanisms that involve the control of phosphorylation and dephosphorylation of Ser, Thr or Tyr residues. Cyclins are molecules that possess a consensus domain called the 'cyclin box.' In mammalian cells, 9 cyclin species have been identified, and they are referred to as cyclins A through I. Cyclin G is a direct transcriptional target of the p53 tumor suppressor gene product and thus functions downstream of p53. GAK is an association partner of cyclin G and CDK5. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Dec 2015]'