Human Lipin 1 (LPIN1) activation kit by CRISPRa

CAT#: GA108097

LPIN1 CRISPRa kit - CRISPR gene activation of human lipin 1



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (3)
LPIN1 mouse monoclonal antibody, clone OTI8F10 (formerly 8F10)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


LPIN1 (Myc-DDK-tagged)-Human lipin 1 (LPIN1)
    • 10 ug

CNY 6,520.00


LPIN1 mouse monoclonal antibody, clone OTI5B5 (formerly 5B5)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol LPIN1
Locus ID 23175
Kit Components

GA108097G1, Lipin 1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA108097G2, Lipin 1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA108097G3, Lipin 1 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Disclaimer These products are manufactured and supplied by OriGene under license from ERS. The kit is designed based on the best knowledge of CRISPRa SAM technology. The efficiency of the activation can be affected by many factors, including nucleosome occupancy status, chromatin structure and the gene expression level of the target, etc.
Reference Data
RefSeq NM_001261427, NM_001261428, NM_001261429, NM_145693, NM_001349199, NM_001349200, NM_001349201, NM_001349202, NM_001349203, NM_001349204, NM_001349205, NM_001349206, NM_001349207, NM_001349208, NR_146080
Synonyms PAP1
Summary This gene encodes a magnesium-ion-dependent phosphatidic acid phosphohydrolase enzyme that catalyzes the penultimate step in triglyceride synthesis including the dephosphorylation of phosphatidic acid to yield diacylglycerol. Expression of this gene is required for adipocyte differentiation and it also functions as a nuclear transcriptional coactivator with some peroxisome proliferator-activated receptors to modulate expression of other genes involved in lipid metabolism. Mutations in this gene are associated with metabolic syndrome, type 2 diabetes, acute recurrent rhabdomyolysis, and autosomal recessive acute recurrent myoglobinuria (ARARM). This gene is also a candidate for several human lipodystrophy syndromes. [provided by RefSeq, Mar 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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