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ABCG2 (BCRP) Antibody (Center)Purified Rabbit Polyclonal Antibody (Pab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AP1490c 0.1 mg 400 ul In Stock $ 255.00 Add to cart
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ABCG2 (BCRP) Antibody (Center) - Product info

ApplicationWB, IF, FC
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionQ9UNQ0
ReactivityHuman
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW72314 Da

ABCG2 (BCRP) Antibody (Center) - Additional info

Gene ID 9429
Other Names
ABCG2; MXR; ABCP; BCRP; BCRP1; ATP-binding cassette sub-family G member 2; Breast cancer resistance protein; CDw338; Mitoxantrone resistance-associated protein; Placenta-specific ATP-binding cassette transporter; CD_antigen=CD338
Target/Specificity
This ABCG2 (BCRP) antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 313~342 amino acids from the center region of human ABCG2.
Dilution
WB~~1:100~500
IF~~1:10~50
FC~~1:10~50
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
ABCG2 (BCRP) Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures.

ABCG2 (BCRP) Antibody (Center) - Protein Information

Name ABCG2
Synonyms ABCP, BCRP, BCRP1, MXR
Function
Xenobiotic transporter that may play an important role in the exclusion of xenobiotics from the brain. May be involved in brain-to-blood efflux. Appears to play a major role in the multidrug resistance phenotype of several cancer cell lines. When overexpressed, the transfected cells become resistant to mitoxantrone, daunorubicin and doxorubicin, display diminished intracellular accumulation of daunorubicin, and manifest an ATP- dependent increase in the efflux of rhodamine 123
Cellular Location
Cell membrane; Multi-pass membrane protein.
Tissue Location
Highly expressed in placenta. Low expression in small intestine, liver and colon

ABCG2 (BCRP) Antibody (Center) - Related products

AP1490b: ABCG2 (BCRP) Antibody (C-term)

AP1490c: ABCG2 (BCRP) Antibody (Center)

RI10030: ABCG2 predesign siRNA

BP1490b: ABCG2 Antibody (C-term) Blocking Peptide

BP1490c: ABCG2 Antibody (Center) Blocking Peptide

ABCG2 (BCRP) Antibody (Center) - Application data

  • Western blot analysis of ABCG2 Antibody (Center) in 293 cell line lysates (35ug/lane). ABCG2(arrow) was detected using the purified Pab (1:60 dilution).

  • Confocal immunofluorescent analysis of ABCG2 (BCRP) Antibody (Center)(Cat#AP1490c) with HepG2 cell followed by Alexa Fluor 488-conjugated goat anti-rabbit lgG (green).DAPI was used to stain the cell nuclear (blue).

  • ABCG2 (BCRP) Antibody (Center) (Cat. #AP1490c) flow cytometric analysis of HepG2 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

ABCG2 (BCRP) Antibody (Center) - Research Areas

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BACKGROUND

ABCG2 is a membrane-associated protein included in the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the White subfamily. Alternatively referred to as a breast cancer resistance protein, this protein functions as a xenobiotic transporter which may play a major role in multi-drug resistance. It likely serves as a cellular defense mechanism in response to mitoxantrone and anthracycline exposure. Significant expression of this protein has been observed in the placenta, which may suggest a potential role for this molecule in placenta tissue.

REFERENCES

Xie,Y., J. Biol. Chem. 283 (6), 3349-3356 (2008) Tamura,A., Drug Metab. Pharmacokinet. 22 (6), 428-440 (2007)