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Alexa Fluor® 647 Mouse Anti-Human CD243 Antibody (S-2907)

Alexa Fluor® 647 Mouse Anti-Human CD243 Antibody (S-2907)

Catalog Number: S0B5663 Application: FCM Reactivity: Human Conjugation: Alexa Fluor® 647 Brand: Starter
Price:
Regular price $185 USD
Regular price Sale price $185 USD
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Product Details

Product Specification


Host Mouse
Antigen CD243
Synonyms ATP-dependent translocase ABCB1; ATP-binding cassette sub-family B member 1; Multidrug resistance protein 1; P-glycoprotein 1; Phospholipid transporter ABCB1; MDR1; PGY1; ABCB1
Location Cytoplasm, Cell membrane
Accession P08183
Clone Number S-2907
Antibody Type Mouse mAb
Isotype IgG2a,k
Application FCM
Reactivity Hu
Positive Sample HepG2
Purification Protein A
Concentration 0.2 mg/ml
Conjugation Alexa Fluor® 647
Physical Appearance Liquid
Storage Buffer

PBS, 1% BSA, 0.3% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, 2 to 8 °C as supplied

Dilution


application dilution species
FCM 5μl per million cells in 100μl volume Hu

Background

CD243, also known as multidrug resistance protein 1 (MDR1) or P-glycoprotein (P-gp), is a 170 kDa transmembrane protein that belongs to the ATP-binding cassette (ABC) transporter family. It functions as an ATP-dependent efflux pump, transporting a wide range of lipophilic compounds, including anti-cancer drugs, out of cells. This protein is expressed on various cell types, such as B cells, T cells, and NK cells, but not on monocytes. CD243 plays a significant role in multidrug resistance in cancer therapy and is involved in the transport of molecules across cellular membranes.

Picture

FC

Flow cytometric analysis of Human CD243 expression on HepG2 cells. Cells from the HepG2 (Human hepatocellular carcinoma epithelial cell) was stained with either Alexa Fluor® 647 Mouse IgG2a, κ Isotype Control (Left panel) or SDT Alexa Fluor® 647 Mouse Anti-Human CD243 Antibody (Right panel) at 5 μl/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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