Human Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Protein

Este producto es parte de ACADM - Acyl-CoA Dehydrogenase C-4 To C-12 Straight Chain
Human Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Protein
234€ (2 µg)

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Name
Human Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Protein
Category
Proteins and Peptides
Provider
Abbexa
Reference
abx073777
Tested Applications
SDS-PAGE

Description

ACADM Protein is a recombinant enzyme.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Proteins and Peptides
Immunogen Target
Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Host
E. coli
Assay Type
Activity: Not tested
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Origin
Human
Expression
Recombinant
Purity
> 90% (SDS-PAGE)
Size 1
2 µg
Size 2
10 µg
Size 3
1 mg
Form
Liquid
Tested Applications
SDS-PAGE
Availability
Shipped within 5-10 working days.
Storage
Store at 4°C if the entire vial will be used within 2-4 weeks. Store at -20 °C for long term storage. For long term storage, it is recommended to add a carrier protein (0.1% HSA or BSA). Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P11310
Alias
ACAD1,MCAD,MCADH
Background
Protein ACADM
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

The ACADM gene encodes the enzyme acyl-Coenzyme A dehydrogenase, specific to medium-chain fatty acids (C4 to C12 straight chain). This enzyme plays a crucial role in the initial step of the mitochondrial fatty acid beta-oxidation pathway, essential for converting medium-chain fatty acids into energy, particularly during fasting periods. Defects in this gene lead to medium-chain acyl-CoA dehydrogenase deficiency, characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can be fatal in infants. ACADM enzyme functions within mitochondria, primarily in the liver, where it aids in the breakdown of medium-chain fatty acids obtained from diet or stored in the body's fat tissue. Alternative splicing generates various isoforms of this enzyme.

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