APC Anti-P Glycoprotein antibody [UIC2]
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Mouse Monoclonal P Glycoprotein antibody - conjugated to APC. Suitable for Flow Cyt and reacts with Human samples. Immunogen corresponding to Cell preparation containing ABCB1 protein.
View Alternative Names
CD243, MDR1, PGY1, ABCB1, ATP-dependent translocase ABCB1, ATP-binding cassette sub-family B member 1, Multidrug resistance protein 1, P-glycoprotein 1, Phospholipid transporter ABCB1
- Flow Cyt
Supplier Data
Flow Cytometry - APC Anti-P Glycoprotein antibody [UIC2] (AB272340)
Flow cytometry surface staining pattern of HepG2 (Human liver hepatocellular carcinoma cell line) cell suspension stained using ab272340 at 10 μl reagent per milion cells in 100 μl of cell suspension. P Glycoprotein also known as CD243.
- Flow Cyt
Supplier Data
Flow Cytometry - APC Anti-P Glycoprotein antibody [UIC2] (AB272340)
Separation of HepG2 (Human liver hepatocellular carcinoma cell line) cells (red-filled) from human peripheral whole blood cells (black-dashed) in flow cytometry analysis (surface staining) stained using ab272340 at 10 μl reagent per milion cells in 100 μl of cell suspension. P Glycoprotein also known as CD243.
Reactivity data
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Supplementary information
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Biological function summary
P-glycoprotein acts as a protective mechanism against toxic substances and drugs within the body. It is a member of the ATP-binding cassette (ABC) transporter family which is critical for their ability to transport molecules across membranes. P-glycoprotein is not typically part of a larger protein complex but can interact with other membrane proteins to facilitate its function. Its role in drug metabolism and excretion is vital for maintaining the balance and elimination of harmful substances.
Pathways
P-glycoprotein plays a significant role in the pharmacokinetics of drugs within the body. This transporter is involved in the multi-drug resistance (MDR) pathway which impacts the efficacy of chemotherapeutic agents. P-glycoprotein also interacts with other proteins like CYP3A4 which is involved in the metabolism of many drugs. These interactions affect the concentration and distribution of therapeutic agents contributing to the body's overall drug response.
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