PPP2R5D (NM_006245) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC201945L2V

Lenti ORF particles, PPP2R5D (mGFP-tagged) - Human protein phosphatase 2, regulatory subunit B', delta (PPP2R5D), transcript variant 1, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: PPP2R5D
• Synonyms: B56D; B56delta; MRD35
• Vector: pLenti-C-mGFP
• ACCN: NM_006245
• ORF Size: 1806 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC201945).
• 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_006245.2, NP_006236.1
• RefSeq Size: 3065 bp
• RefSeq ORF: 1809 bp
• Locus ID: 5528
• Cytogenetics: 6p21.1
• Domains: B56
• Protein Families: Phosphatase
• Protein Pathways: Oocyte meiosis, Wnt signaling pathway
• MW: 70 kDa
• Gene Summary: 'The product of this gene belongs to the phosphatase 2A regulatory subunit B family. Protein phosphatase 2A is one of the four major Ser/Thr phosphatases, and it is implicated in the negative control of cell growth and division. It consists of a common heteromeric core enzyme, which is composed of a catalytic subunit and a constant regulatory subunit, that associates with a variety of regulatory subunits. The B regulatory subunit might modulate substrate selectivity and catalytic activity. This gene encodes a delta isoform of the regulatory subunit B56 subfamily. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]'