PPM1A (NM_177952) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC229231L4V
- LentiORF®
-
Lenti ORF particles, PPM1A (mGFP-tagged) - Human protein phosphatase, Mg2+/Mn2+ dependent, 1A (PPM1A), transcript variant 3, 200ul, >10^7 TU/mL
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CNY 9,975.00
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Specifications
Product Data | |
Product Name | PPM1A (NM_177952) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | PP2C-ALPHA; PP2CA; PP2Calpha |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_177952 |
ORF Size | 1365 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC229231).
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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_177952.2 |
RefSeq ORF | 1368 bp |
Locus ID | 5494 |
Protein Families | Druggable Genome, Phosphatase |
Protein Pathways | MAPK signaling pathway |
MW | 51.2 kDa |
Gene Summary | The protein encoded by this gene is a member of the PP2C family of Ser/Thr protein phosphatases. PP2C family members are known to be negative regulators of cell stress response pathways. This phosphatase dephosphorylates, and negatively regulates the activities of, MAP kinases and MAP kinase kinases. It has been shown to inhibit the activation of p38 and JNK kinase cascades induced by environmental stresses. This phosphatase can also dephosphorylate cyclin-dependent kinases, and thus may be involved in cell cycle control. Overexpression of this phosphatase is reported to activate the expression of the tumor suppressor gene TP53/p53, which leads to G2/M cell cycle arrest and apoptosis. Three alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Jul 2008] |
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