Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Antibody (Biotin)

Este producto es parte de ACADM - Acyl-CoA Dehydrogenase C-4 To C-12 Straight Chain
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416€ (200 µl)

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935106861
info@markelab.com
name
Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM) Antibody (Biotin)
category
Primary Antibodies
provider
Abbexa
reference
abx432270
tested applications
P-ELISA, WB

Description

ACADM Antibody is a Goat Polyclonal antibody against ACADM (

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Acyl-CoA Dehydrogenase, C-4 To C-12 Straight Chain (ACADM)
Host
Goat
Reactivity
Human
Recommended Dilution
P-ELISA: 1/16000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Biotin
Isotype
IgG
Purification
Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Size 1
200 µl
Form
Liquid
Tested Applications
P-ELISA, WB
Buffer
Tris saline, pH 7.3, containing 0.02% sodium azide and 0.5% bovine serum albumin.
Availability
Shipped within 1-3 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Gene ID
34
NCBI Accession
NP_000007.1, NP_001120800.1, NP_001272971.1, NP_001272972.1, NP_001272973.1
Alias
ACAD1,MCAD,MCADH
Background
Antibody anti-ACADM
Status
RUO
Note
Concentration: 0.5 mg/ml - 

Descripción

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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