ABCC2 KO cell lysate available now. KO validated by Next Generation Sequencing, Western blot. Free of charge wild type control included. Knockout achieved by CRISPR/Cas9 X = 11 bp deletion Frameshift = 97%.
ABC30, ATP binding cassette sub family C (CFTR/MRP) member 2, ATP-binding cassette sub-family C member 2, CMOAT, CMOAT1, Canalicular multidrug resistance protein, Canalicular multispecific organic anion transporter 1, DJS, KIAA1010, MRP2_HUMAN, Multidrug resistance-associated protein 2, abcC2, cMRP
ABCC2 KO cell lysate available now. KO validated by Next Generation Sequencing, Western blot. Free of charge wild type control included. Knockout achieved by CRISPR/Cas9 X = 11 bp deletion Frameshift = 97%.
Knockout cell lysate achieved by CRISPR/Cas9.
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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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MRP2 also known as ABCC2 or MRP-2 transporter is an ATP-binding cassette transporter. This protein with a molecular mass of about 190 kDa is widely expressed in tissues such as the liver kidney and intestine. MRP2 plays a role in drug and metabolite transport moving various organic anions across cellular membranes. It locates to the canalicular membrane of hepatocytes where it functions in secreting conjugated bilirubin and drugs into bile.
MRP2 contributes to cellular detoxification processes. It does not form part of a larger protein complex but works as an independent entity. MRP2 protein actively transports conjugated substances out of cells protecting tissues from potential damage from toxins drugs and other organic anions. This transporter mediates the excretion of glucuronide sulfate and glutathione conjugates playing an important role in phase III of drug metabolism.
MRP2 transporter is integral to xenobiotic metabolism. It interconnects with the conjugation pathways that prepare compounds for excretion. The pathway functions with cytochrome P450 enzymes and other related transport proteins like MDR1 facilitating the secretion of detoxified metabolites. MRP2 activity influences pharmacokinetics and pharmacodynamics by modulating drug disposition and excretion.
MRP2 is associated with Dubin-Johnson syndrome and cholestasis. Dubin-Johnson syndrome arises from mutations in the ABCC2 gene leading to defective bilirubin excretion and jaundice. Cholestasis involves impaired bile excretion where MRP2 and possibly related proteins like BSEP play roles in bile salt export. Understanding MRP2 functioning aids in assessing risk and treatment strategies for these conditions.
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Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate 20 ug
Lane 4: HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4: Merged signal (red and green). Green - Anti-MRP2 antibody [EPR10998] ab172630 observed at 210 kDa. Red - loading control, Anti-Vinculin antibody [VIN-54] ab130007, observed at 130 kDa.
Anti-MRP2 antibody [EPR10998] ab172630 was shown to recognize MRP2 in wild-type A549 cells as signal was lost at the expected MW in ABCC2 knockout cell line Human ABCC2 knockout A549 cell line ab261855 (knockout cell lysate ab261663). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and ABCC2 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. Anti-MRP2 antibody [EPR10998] ab172630 and Anti-Vinculin antibody [VIN-54] ab130007 (Mouse anti-Vinculin loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/1000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-MRP2 antibody [EPR10998] (Anti-MRP2 antibody [EPR10998] ab172630) at 1/1000 dilution
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: Western blot - Human ABCC2 knockout A549 cell line (Human ABCC2 knockout A549 cell line ab261855)
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 20 µg
Lane 4: HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 174 kDa
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate
Lanes 1 - 2: Merged signal (red and green). Green - Anti-MRP2 antibody [M2III-5] ab15603 observed at 210 kDa. Red - loading control, Anti-alpha Tubulin antibody [EP1332Y] - Loading Control ab52866, observed at 50 kDa.
Anti-MRP2 antibody [M2III-5] ab15603 was shown to recognize ABCC2 in wild-type A549 cells as signal was lost at the expected MW in ABCC2 knockout cell line Human ABCC2 knockout A549 cell line ab261855 (knockout cell lysate ab261663). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and ABCC2 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. Anti-MRP2 antibody [M2III-5] ab15603 and Anti-alpha Tubulin antibody [EP1332Y] - Loading Control ab52866 (Rabbit anti-alpha Tubulin loading control) were incubated overnight at 4°C at 1/20 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772 and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-MRP2 antibody [M2III-5] (Anti-MRP2 antibody [M2III-5] ab15603) at 1/20 dilution
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: Western blot - Human ABCC2 knockout A549 cell line (Human ABCC2 knockout A549 cell line ab261855)
Performed under reducing conditions.
Predicted band size: 174 kDa
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate 20 ug
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate 20 ug
Lane 4: HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate 20 ug
Lanes 1 - 4: Merged signal (red and green). Green - Anti-MRP2 antibody [EPR10997(2)] ab187644 observed at 210 kDa. Red - loading control, Anti-Vinculin antibody [VIN-54] ab130007, observed at 130 kDa.
Anti-MRP2 antibody [EPR10997(2)] ab187644 was shown to recognize MRP2 in wild-type A549 cells as signal was lost at the expected MW in ABCC2 knockout cell line Human ABCC2 knockout A549 cell line ab261855 (knockout cell lysate ab261663). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and ABCC2 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. Anti-MRP2 antibody [EPR10997(2)] ab187644 and Anti-Vinculin antibody [VIN-54] ab130007 (Mouse anti-Vinculin loading control) were incubated overnight at 4°C at 1/1000 dilution and 1/1000 dilution respectively. Blots were developed with Goat anti-Rabbit IgG H&L (IRDye® 800CW) preabsorbed Goat anti-Rabbit IgG H&L (IRDye® 800CW) preadsorbed ab216773 and Goat anti-Mouse IgG H&L (IRDye® 680RD) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 680RD) preadsorbed ab216776 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-MRP2 antibody [EPR10997(2)] (Anti-MRP2 antibody [EPR10997(2)] ab187644) at 1/1000 dilution
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: Western blot - Human ABCC2 knockout A549 cell line (Human ABCC2 knockout A549 cell line ab261855)
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 20 µg
Lane 4: HeLa (Human epithelial cell line from cervix adenocarcinoma) whole cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 174 kDa
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate
Lanes 1 - 3: Merged signal (red and green). Green - Anti-MRP2 antibody [M2 III-6] ab3373 observed at 210 kDa. Red - loading control, Anti-alpha Tubulin antibody [EP1332Y] - Loading Control ab52866, observed at 50 kDa.
Anti-MRP2 antibody [M2 III-6] ab3373 was shown to recognize ABCC2 in wild-type A549 cells as signal was lost at the expected MW in ABCC2 knockout cell line Human ABCC2 knockout A549 cell line ab261855 (knockout cell lysate ab261663). Additional cross-reactive bands were observed in the wild-type and knockout samples. Wild-type and ABCC2 knockout samples were subjected to SDS-PAGE. The membrane was blocked with 3% milk. Anti-MRP2 antibody [M2 III-6] ab3373 and Anti-alpha Tubulin antibody [EP1332Y] - Loading Control ab52866 (Rabbit anti-alpha Tubulin loading control) were incubated overnight at 4°C at 1/20 dilution and 1/20000 dilution respectively. Blots were developed with Goat anti-Mouse IgG H&L (IRDye® 800CW) preabsorbed Goat anti-Mouse IgG H&L (IRDye® 800CW) preadsorbed ab216772 and Goat anti-Rabbit IgG H&L (IRDye® 680RD) preabsorbed Goat Anti-Rabbit IgG H&L (IRDye® 680RD) preadsorbed ab216777 secondary antibodies at 1/20000 dilution for 1 hour at room temperature before imaging.
All lanes: Western blot - Anti-MRP2 antibody [M2 III-6] (Anti-MRP2 antibody [M2 III-6] ab3373) at 1/20 dilution
Lane 1: Wild-type A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: ABCC2 knockout A549 (Human lung carcinoma cell line) whole cell lysate at 20 µg
Lane 2: Western blot - Human ABCC2 knockout A549 cell line (Human ABCC2 knockout A549 cell line ab261855)
Lane 3: Hep G2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 20 µg
Performed under reducing conditions.
Predicted band size: 174 kDa
X = 11 bp deletion
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