Human AMPD1 activation kit by CRISPRa

CAT#: GA100185

AMPD1 CRISPRa kit - CRISPR gene activation of human adenosine monophosphate deaminase 1



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CNY 12,255.00


货期*
4周

规格
    • 1 kit

Product images

经常一起买 (2)
Rabbit Polyclonal Anti-AMPD1 Antibody
    • 100 ul

CNY 1,999.00
CNY 3,280.00


AMPD1 (Myc-DDK-tagged)-Human adenosine monophosphate deaminase 1 (AMPD1), transcript variant 1
    • 10 ug

CNY 5,472.00
CNY 8,270.00

Specifications

Product Data
Format 3 gRNAs (5ug each), 1 scramble ctrl (10ug) and 1 enhancer vector (10ug)
Symbol AMPD1
Locus ID 270
Kit Components

GA100185G1, AMPD1 gRNA vector 1 in pCas-Guide-GFP-CRISPRa

GA100185G2, AMPD1 gRNA vector 2 in pCas-Guide-GFP-CRISPRa

GA100185G3, AMPD1 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_000036, NM_001172626
Synonyms MAD; MADA; MMDD
Summary Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
*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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