Pyruvate Dehydrogenase Complex Component X (PDHX) Antibody

Este producto es parte de PDHX - Pyruvate dehydrogenase protein X
Pyruvate Dehydrogenase Complex Component X (PDHX) Antibody
234€ (5 µg)

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Name
Pyruvate Dehydrogenase Complex Component X (PDHX) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx137680

Description

Pyruvate Dehydrogenase Complex Component X (PDHX) Antibody is a Mouse Monoclonal antibody against Pyruvate Dehydrogenase Complex Component X (PDHX).

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Pyruvate Dehydrogenase Complex Component X (PDHX)
Host
Mouse
Reactivity
Human
Clonality
Monoclonal
Size 1
5 µg
Size 2
20 µg
Size 3
100 µg
Availability
Shipped within 5-10 working days.
Dry Ice
No
Alias
DLDBP, E3BP, OPDX, PDX1, proX, pyruvate dehydrogenase complex component X, PDHXD
Background
Antibody anti-PDHX
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.

Background

PDHX is a component of the pyruvate dehydrogenase complex (PDC) located in the mitochondrial matrix, where it plays a critical role in linking glycolysis to the tricarboxylic acid (TCA) cycle by catalyzing the conversion of pyruvate to acetyl-CoA. PDHX functions as the E3-binding protein, anchoring dihydrolipoamide dehydrogenase (E3) to the PDC core and facilitating the transfer of reducing equivalents between PDC subunits. It is essential for the stability and activity of the PDC, ensuring efficient energy production and metabolic homeostasis. Mutations in PDHX are associated with pyruvate dehydrogenase deficiency, a condition characterized by lactic acidosis, developmental delay, and neurological dysfunction due to impaired mitochondrial energy metabolism. PDHX is expressed ubiquitously in energy-demanding tissues such as the brain, muscle, and liver, where it supports ATP production and metabolic adaptation. Knockout studies demonstrate reduced PDC activity, metabolic imbalances, and severe defects in energy-dependent processes, underscoring its importance in cellular respiration and energy metabolism.

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