Phospholipid-transporting ATPase ABCA3 (ABCA3) Antibody

Este producto es parte de ABCA3 - ATP Binding Cassette Transporter A3
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260€ (50 µl)

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935106861
info@markelab.com
name
Phospholipid-transporting ATPase ABCA3 (ABCA3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx340981
tested applications
ELISA, WB, IF/ICC

Description

Phospholipid-transporting ATPase ABCA3 (ABCA3) Antibody is a Rabbit Polyclonal antibody for the detection of Human ABCA3.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Target: Phospholipid-transporting ATPase ABCA3 (ABCA3)
Immunogen: Synthetic peptide of human ABCA3
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/1000 - 1/5000, IF/ICC: 1/20 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified from antiserum by affinity chromatography using epitope-specific immunogen.
Size 1
50 µl
Size 2
100 µl
Form
Liquid
Tested Applications
ELISA, WB, IF/ICC
Buffer
PBS, pH 7.4, containing 0.05% NaN3, 40% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q99758
Gene ID
21
OMIM
601615
Alias
ABC-C,ABC3,LBM180,SMDP3
Background
Antibody anti-ABCA3
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

ABCA3 is a critical protein in pulmonary surfactant production, predominantly expressed in alveolar type II epithelial cells in the lungs. It plays an essential role in transporting phospholipids and cholesterol into lamellar bodies, which are specialized organelles where surfactant is stored before secretion. ABCA3 utilizes ATP hydrolysis to facilitate lipid transport, ensuring the proper composition and function of surfactant, which reduces surface tension in the alveoli and prevents lung collapse. Mutations in the ABCA3 gene are associated with surfactant metabolism disorders, including neonatal respiratory distress syndrome and interstitial lung disease. These conditions are characterized by impaired surfactant production, leading to respiratory failure. ABCA3’s function in lipid transport and its critical role in pulmonary physiology underscore its importance in respiratory health.

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