SLC9A3R2 KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 11 bp deletion in exon 3.
E3KARP, HGNC:11076, Isoform 3 regulator 2, Isoform 3 regulatory factor 2, MGC104639, NHE3 kinase A regulatory protein, NHE3 kinase A regulatory protein E3KARP, NHE3 regulatory factor 2, NHE3RF2, NHERF-2, NHRF2_HUMAN, Na(+)/H(+) exchange regulatory cofactor NHE-RF2, OCTS2, SIP-1, SRY-interacting protein 1, Slc9a3r2, Sodium-hydrogen exchanger regulatory factor 2, Sodium/hydrogen exchanger, Sodium/hydrogen exchanger regulatory factor 2, Solute carrier family 9 (sodium/hydrogen exchanger), Solute carrier family 9 (sodium/hydrogen exchanger) isoform 3 regulator 2, Solute carrier family 9 (sodium/hydrogen exchanger) isoform 3 regulatory factor 2, Solute carrier family 9 (sodium/hydrogen exchanger) member 3 regulator 2, Solute carrier family 9 isoform 3 regulator 2, Solute carrier family 9 isoform A3 regulatory factor 2, TKA-1, Tyrosine kinase activator protein 1
SLC9A3R2 KO cell lysate available now. KO validated by Western blot. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 11 bp deletion in exon 3.
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Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.
User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.
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Anti-NHERF-2/SIP-1 antibody [32B6] ab151443 was shown to specifically react with NHERF-2/SIP-1 in wild-type HEK293T cells. Loss of signal was observed when knockout cell line Human SLC9A3R2 (NHERF-2/SIP-1) knockout HEK-293T cell line ab266778 (knockout cell lysate ab258685) was used. Wild-type and NHERF-2/SIP-1 knockout samples were subjected to SDS-PAGE. Anti-NHERF-2/SIP-1 antibody [32B6] ab151443 and Anti-beta Tubulin [EP1331Y] - Microtubule Marker (Anti-beta Tubulin antibody [EP1331Y] - Microtubule Marker ab52901) were incubated overnight at 4oC at 1 in 500 dilution and 1 in 20000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed (Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777) and Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed (Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772) secondary antibodies at 1 in 20000 dilution for 1 hour at room temperature before imaging.
Homozygous: 11 bp deletion in exon 3
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