Acid Phosphatase 2 (ACP2) (NM_001610) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC210562L3V

  • LentiORF®

Lenti ORF particles, ACP2 (Myc-DDK-tagged)-Human acid phosphatase 2, lysosomal (ACP2), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 8,930.00


货期*
详询

规格
    • 200 ul

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Specifications

Product Data
Product Name Acid Phosphatase 2 (ACP2) (NM_001610) Human Tagged ORF Clone Lentiviral Particle
Synonyms LAP
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_001610
ORF Size 1270 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC210562).
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_001610.1
RefSeq Size 2218 bp
RefSeq ORF 1272 bp
Locus ID 53
Domains acid_phosphat
Protein Families Druggable Genome, Transmembrane
Protein Pathways Lysosome, Riboflavin metabolism
MW 44.45 kDa
Gene Summary The protein encoded by this gene belongs to the histidine acid phosphatase family, which hydrolyze orthophosphoric monoesters to alcohol and phosphate. This protein is localized to the lysosomal membrane, and is chemically and genetically distinct from the red cell acid phosphatase. Mice lacking this gene showed multiple defects, including bone structure alterations, lysosomal storage defects, and an increased tendency towards seizures. An enzymatically-inactive allele of this gene in mice showed severe growth retardation, hair-follicle abnormalities, and an ataxia-like phenotype. Alternatively spliced transcript variants have been found for this gene. A C-terminally extended isoform is also predicted to be produced by the use of an alternative in-frame translation termination codon via a stop codon readthrough mechanism. [provided by RefSeq, Oct 2017]
*Delivery time may vary from web posted schedule. Occasional delays may occur due to unforeseen complexities in the preparation of your product. International customers may expect an additional 1-2 weeks in shipping.
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