Adenosine A1-R Antibody (D-5) Alexa Fluor® 790: sc-514337 AF790. Direct near-infrared western blot analysis of Adenosine A1-R expression in MCF7 (A), K-562 (B) and U-2 OS (C) whole cell lysates. Blocked with UltraCruz® Blocking Reagent: sc-516214.
Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
Adenosine A1-R Antibody (D-5) Alexa Fluor® 790: sc-514337 AF790. Direct near-infrared western blot analysis of Adenosine A1-R expression in MCF7 (A), K-562 (B) and U-2 OS (C) whole cell lysates. Blocked with UltraCruz® Blocking Reagent: sc-516214.
Not CRISPR data: the image illustrates antibody quality for visualizing CRISPR experiment results.
20 µg of transfection-ready, purified plasmid DNA; Suitable for up to 20 transfections
Adenosine A1-R CRISPR Activation Plasmid (h) is a synergistic activation mediator (SAM) transcription activation system designed to specifically upregulate gene expression
Adenosine A1-R CRISPR Activation Plasmid (h) consists of three plasmids at a 1:1:1 mass ratio: a plasmid encoding the deactivated Cas9 (dCas9) nuclease (D10A and N863A) fused to the transactivation domain VP64, and a blasticidin resistance gene; a plasmid encoding the MS2-p65-HSF1 fusion protein, and a hygromycin resistance gene; a plasmid encoding a target-specific 20 nt guide RNA fused to two MS2 RNA aptamers, and a puromycin resistance gene
The resulting SAM complex binds to a site-specific region approximately 200-250 nt upstream of the transcriptional start site and provides robust recruitment of transcription factors for highly efficient gene activation
gRNAs encoded by Adenosine A1-R CRISPR Activation Plasmid (h) and Adenosine A1-R CRISPR Activation Plasmid (h2) target distinct regulatory regions upstream of the ADORA1 transcriptional start site. One or both designs may be available
Following transfection, gene knockout efficiency can be assayed by WB, IF or IHC using antibody: Adenosine A1-R Antibody (D-5): sc-514337