Perilipin-1 (PLIN1) (NM_002666) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC206292L4V

  • LentiORF®

Lenti ORF particles, PLIN1 (mGFP-tagged) - Human perilipin 1 (PLIN1), transcript variant 1, 200ul, >10^7 TU/mL

ORF Plasmid: DDK tGFP



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CNY 9,975.00


货期*
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规格
    • 200 ul

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Specifications

Product Data
Product Name Perilipin-1 (PLIN1) (NM_002666) Human Tagged ORF Clone Lentiviral Particle
Synonyms FPLD4; PERI; PLIN
Vector pLenti-C-mGFP-P2A-Puro
ACCN NM_002666
ORF Size 1566 bp
Sequence Data
The ORF insert of this clone is exactly the same as(RC206292).
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_002666.3
RefSeq Size 2922 bp
RefSeq ORF 1569 bp
Locus ID 5346
Domains perilipin
Protein Families Druggable Genome
Protein Pathways PPAR signaling pathway
MW 55.8 kDa
Gene Summary The protein encoded by this gene coats lipid storage droplets in adipocytes, thereby protecting them until they can be broken down by hormone-sensitive lipase. The encoded protein is the major cAMP-dependent protein kinase substrate in adipocytes and, when unphosphorylated, may play a role in the inhibition of lipolysis. Alternatively spliced transcript variants varying in the 5' UTR, but encoding the same protein, have been found for this gene. [provided by RefSeq, Feb 2009]
*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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