Mouse Atf4 activation kit by CRISPRa

CAT#: GA200307

Atf4 CRISPRa kit - CRISPR gene activation of mouse activating transcription factor 4



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CN¥ 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
Atf4 Antibody - N-terminal region
    • 100 ul

CN¥ 5,250.00


ATF4 Antibody - middle region
    • 50 ug

CN¥ 4,628.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol Atf4
Locus ID 11911
Kit Components

GA200307G1, Atf4 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA200307G2, Atf4 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA200307G3, Atf4 gRNA vector 3 in pCas-Guide-GFP-CRISPRa

1 CRISPRa-Enhancer vector, SKU GE100056

1 CRISPRa scramble vector, SKU GE100077

Reference Data
RefSeq NM_001287180, NM_009716
Synonyms Atf-4; C/ATF; CREB2; TAXREB67
Summary Transcriptional activator. Binds the cAMP response element (CRE) (consensus: 5'-GTGACGT[AC][AG]-3'), a sequence present in many viral and cellular promoters. Binds to asymmetric CRE's as a heterodimer and to palindromic CRE's as a homodimer. Cooperates with FOXO1 in osteoblasts to regulate glucose homeostasis through suppression of beta-cell production and decrease in insulin production. Regulates the induction of DDIT3/CHOP and asparagine synthetase (ASNS) in response to ER stress. In concert with DDIT3/CHOP, activates the transcription of TRIB3 and promotes ER stress-induced neuronal apoptosis by regulating the transcriptional induction of BBC3/PUMA. Activates transcription of SIRT4. Regulates the circadian expression of the core clock component PER2 and the serotonin transporter SLC6A4. Binds in a circadian time-dependent manner to the cAMP response elements (CRE) in the SLC6A4 and PER2 promoters and periodically activates the transcription of these genes.[UniProtKB/Swiss-Prot Function]
*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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