Human Cytochrome P450 Reductase (POR) activation kit by CRISPRa

CAT#: GA103670

POR CRISPRa kit - CRISPR gene activation of human cytochrome p450 oxidoreductase



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Cited in 1 publication.

Product images

经常一起买 (3)
POR (Cytochrome P450 Reductase) mouse monoclonal antibody, clone OTI5B3 (formerly 5B3)
    • 100 ul

CNY 1,999.00
CNY 2,700.00


POR (Myc-DDK-tagged)-Human P450 (cytochrome) oxidoreductase (POR)
    • 10 ug

CNY 4,984.00


POR (Cytochrome P450 Reductase) mouse monoclonal antibody, clone OTI3F10 (formerly 3F10)
    • 30 ul

CNY 800.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol POR
Locus ID 5447
Kit Components

GA103670G1, Cytochrome P450 Reductase gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA103670G2, Cytochrome P450 Reductase gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA103670G3, Cytochrome P450 Reductase 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_000941, NM_001367562
Synonyms CPR; CYPOR; P450R
Summary This gene encodes an endoplasmic reticulum membrane oxidoreductase that is essential for multiple metabolic processes, including reactions catalyzed by cytochrome P450 proteins for metabolism of steroid hormones, drugs and xenobiotics. The encoded protein has a flavin adenine dinucleotide (FAD)-binding domain and a flavodoxin-like domain which bind two cofactors, FAD and FMN, that allow it to donate electrons directly from NADPH to all microsomal P450 enzymes. Mutations in this gene cause a complex set of disorders, including apparent combined P450C17 and P450C21 deficiency, amenorrhea and disordered steroidogenesis, congenital adrenal hyperplasia and Antley-Bixler syndrome, that resemble those caused by defects in steroid metabolizing enzymes such as aromatase, 21-hydroxylase, and 17 alpha-hydroxylase. [provided by RefSeq, Aug 2020]
*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.

Citations (1)

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