Pparg (NM_001127330) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR227473L4V
- LentiORF®
Lenti ORF particles, Pparg (GFP-tagged) - Mouse peroxisome proliferator activated receptor gamma (Pparg), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 10,260.00
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Specifications
Product Data | |
Product Name | Pparg (NM_001127330) Mouse Tagged ORF Clone Lentiviral Particle |
Synonyms | Nr1; Nr1c3; PPA; PPAR; Ppar-; PPAR-gamma; PPAR-gamma2; PPARgamma; PPARgamma2 |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001127330 |
ORF Size | 1425 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR227473).
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OTI Disclaimer | Due to the inherent nature of this plasmid, standard methods to replicate additional amounts of DNA in E. coli are highly likely to result in mutations and/or rearrangements. Therefore, OriGene does not guarantee the capability to replicate this plasmid DNA. Additional amounts of DNA can be purchased from OriGene with batch-specific, full-sequence verification at a reduced cost. Please contact our customer care team at custsupport@origene.com or by calling 301.340.3188 option 3 for pricing and delivery. 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_001127330.1 |
RefSeq Size | 1857 bp |
RefSeq ORF | 1428 bp |
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] |
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