Pparg (NM_011146) Mouse Tagged ORF Clone Lentiviral Particle

CAT#: MR208132L3V

  • LentiORF®

Lenti ORF particles, Pparg (Myc-DDK-tagged) - Mouse peroxisome proliferator activated receptor gamma (Pparg), transcript variant 2, 200ul, >10^7 TU/mL



Interest in protein/lysate? Submit request here!

Buy this product and get 50% off on the Lenti RapidTiter kit. Use Code: Rapid50

USD 880.00

6 Weeks*

Size
    • 200 ul

Product Images

Other products for "Pparg"

Specifications

Product Data
Type Mouse Tagged ORF Clone
Tag Myc-DDK
Symbol Pparg
Synonyms Nr1c3; PPAR-gamma; PPAR-gamma2; PPARgamma; PPARgamma2
Mammalian Cell Selection Puromycin
Vector pLenti-C-Myc-DDK-P2A-Puro
ACCN NM_011146
ORF Size 1515 bp
Sequence Data
The ORF insert of this clone is exactly the same as(MR208132).
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_011146.1, NP_035276.1
RefSeq Size 1780
RefSeq ORF 1518
Locus ID 19016
Gene Summary This gene encodes a nuclear receptor protein belonging to the peroxisome proliferator-activated receptor (Ppar) family. The encoded protein is a ligand-activated transcription factor that is involved in the regulation of adipocyte differentiation and glucose homeostasis. The encoded protein forms a heterodimer with retinoid X receptors and binds to DNA motifs termed "peroxisome proliferator response elements" to either activate or inhibit gene expression. Mice lacking the encoded protein die at an embryonic stage due to severe defects in placental vascularization. When the embryos lacking this gene are supplemented with healthy placentas, the mutants survive to term, but succumb to lipodystrophy and multiple hemorrhages. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2015]

{0} Product Review(s)

0 Product Review(s) Submit review

Be the first one to submit a review

Product Citations

*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.