ATP-Dependent Translocase ABCB1 (ABCB1) Antibody

Este producto es parte de ABCB - ATP binding cassette subfamily B member
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351€ (100 µg)

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935106861
info@markelab.com
name
ATP-Dependent Translocase ABCB1 (ABCB1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx414457
tested applications
IHC, IF/ICC, FCM, IP

Description

ATP Binding Cassette Subfamily B Member 1 (ABCB1) Antibody is a Mouse Monoclonal antibody against CD243.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
ATP-Dependent Translocase ABCB1 (ABCB1)
Host
Mouse
Reactivity
Human
Recommended Dilution
Validated in IHC-F and IHC-P. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
Unconjugated
Isotype
IgG2a
Purification
Purified
Size 1
100 µg
Form
Liquid
Tested Applications
IHC, IF/ICC, FCM, IP
Buffer
PBS. Contains sodium azide.
Availability
Shipped within 3-7 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P08183
Alias
ABC20,CD243,CLCS,GP170,MDR1,P-GP,PGY1,p-170
Background
Antibody anti-ABCB1
Status
RUO
Note
Concentration: 1.0 mg/ml - 

Descripción

ABCB1, also known as P-glycoprotein, is a well-studied ATP-dependent efflux transporter involved in the transport of a wide range of substrates, including drugs, lipids, and xenobiotics. It is highly expressed in barrier tissues, such as the blood-brain barrier, intestines, liver, and kidneys, where it functions to protect tissues by actively exporting toxic compounds and drugs. ABCB1 plays a crucial role in pharmacokinetics, influencing drug absorption, distribution, and elimination. Overexpression of ABCB1 in cancer cells is a major contributor to multidrug resistance, as it pumps chemotherapeutic agents out of cells, reducing their efficacy. Structurally, ABCB1 contains two transmembrane domains and two ATP-binding domains, which utilize ATP hydrolysis to drive substrate transport. Its pivotal role in drug resistance and detoxification makes it a significant target in cancer therapy and pharmacological research.

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