ACADL anticorps (N-Term)

N° du produit ABIN2778158

Cet anticorps Lapin Polyclonal détecte spécifiquement ACADL dans WB. Il présente une réactivité envers Humain, Souris, Rat, Cheval, Porc, Lapin, Boeuf (Vache) et Chien.

Aperçu rapide pour ACADL anticorps (N-Term) (ABIN2778158)

Antigène: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Reactivité: Humain, Souris, Rat, Cheval, Porc, Lapin, Boeuf (Vache), Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACADL est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ACADL anticorps

Épitope: N-Term

Séquence: MAARLLRGSL RVLGGHRAPR QLPAARCSHS GGEERLETPS AKKLTDIGIR

Homologie: Cow: 93%, Dog: 86%, Horse: 100%, Human: 100%, Mouse: 92%, Pig: 93%, Rabbit: 85%, Rat: 92%

Attributs du produit: This is a rabbit polyclonal antibody against ACADL. It was validated on Western Blot using a cell lysate as a positive control.

Purification: Affinity Purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human ACADL

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 430 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur ACADL

Antigène: ACADL (Acyl-CoA Dehydrogenase, Long Chain (ACADL))

Autre désignation: ACADL

Sujet: ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in ACADL gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.
Alias Symbols: ACAD4, LCAD
Protein Interaction Partner: Htt, UBC,
Protein Size: 430

Poids moléculaire: 44 kDa

ID gène: 33

NCBI Accession: NM_001608, NP_001599

UniProt: P28330

Pathways: Monocarboxylic Acid Catabolic Process