Aph1a (NM_146134) Mouse Tagged ORF Clone Lentiviral Particle

CAT#: MR220937L4V

  • LentiORF®

Lenti ORF particles, Aph1a (GFP-tagged) - Mouse anterior pharynx defective 1a homolog (C. elegans) (Aph1a), transcript variant 2, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,360.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name Aph1a (NM_146134) Mouse Tagged ORF Clone Lentiviral Particle
Synonyms 6530402N02Rik; APH-1a
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_146134
ORF Size 795 bp
Sequence Data
The ORF insert of this clone is exactly the same as(MR220937).
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_146134.2, NP_666246.1
RefSeq Size 2882 bp
RefSeq ORF 798 bp
Locus ID 226548
Gene Summary This gene encodes a subunit of the gamma-secretase complex, which is localized to the endoplasmic reticulum and golgi apparatus. Gamma-secretase is a multi-protein enzyme that catalyzes intramembraneous proteolysis of type I transmembrane proteins and is essential for many signaling pathways, including the Notch signaling pathway. Studies suggest that the protein encoded by this locus binds directly to substrates of the gamma-secretase complex, including the beta-amyloid precursor protein which is associated with Alzheimer disease progression. This gene is required for normal embryonic development and survival, and disruption is associated with defects in the yolk sack angiogenesis, neural tube formation, and somitogenesis. A pseudogene of this gene is located on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]
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