ATP Binding Cassette Transporter A3 (ABCA3) Antibody

Este producto es parte de ABCA3 - ATP Binding Cassette Transporter A3
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357.5€ (100 µg)

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935106861
info@markelab.com
name
ATP Binding Cassette Transporter A3 (ABCA3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx340255
tested applications
ELISA, WB

Description

Rabbit Polyclonal against the ABCA3 protein. This product is a carrier-free, azide-free and glycerol-free form of the

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetATP Binding Cassette Transporter A3 (ABCA3)
HostRabbit
ReactivityHuman
Recommended DilutionELISA: 1/20000 - 1/80000, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
IsotypeIgG
PurificationPurified by antigen affinity column chromatography.
Size 1100 µg
Size 21 mg
FormLyophilized
Tested ApplicationsELISA, WB
BufferDoes not contain sodium azide, carrier proteins, or glycerol.
AvailabilityShipped within 7-15 working days.
StorageStore at -20 °C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ99758
Gene ID21
OMIM601615
AliasABC-C,ABC3,LBM180,SMDP3
BackgroundAntibody anti-ABCA3
StatusRUO
NoteConcentration: Not applicable. -

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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