EHHADH anticorps (Middle Region)

N° du produit ABIN5514454

L’anticorps anti-EHHADH Polyclonal Lapin est utilisé pour la détection de EHHADH dans des échantillons de Humain. Il a été validé pour WB.

Aperçu rapide pour EHHADH anticorps (Middle Region) (ABIN5514454)

Antigène: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp EHHADH est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-EHHADH anticorps

Épitope: Middle Region

Fonction: EHHADH Antibody - middle region

Séquence: VIAVDSDKNQ LATANKMITS VLEKEASKMQ QSGHPWSGPK PRLTSSVKEL

Attributs du produit: This is a rabbit polyclonal antibody against ECHP. It was validated on Western Blot.

Purification: Affinity purified

Immunogène: The immunogen is a synthetic peptide directed towards the middle region of Human ECHP

Information d'application

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

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP76113-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: 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: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

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

Détails sur EHHADH

Antigène: EHHADH (Enoyl-CoA, Hydratase/3-Hydroxyacyl CoA Dehydrogenase (EHHADH))

Autre désignation: EHHADH

Sujet:

Background Information: The protein encoded by this gene is a bifunctional enzyme and is one of the four enzymes of the peroxisomal beta-oxidation pathway. The N-terminal region of the encoded protein contains enoyl-CoA hydratase activity while the C-terminal region contains 3-hydroxyacyl-CoA dehydrogenase activity. Defects in this gene are a cause of peroxisomal disorders such as Zellweger syndrome. Two transcript variants encoding different isoforms have been found for this gene.

Gene Name: enoyl-CoA hydratase and 3-hydroxyacyl CoA dehydrogenase

Alternative Symbols: LBP, ECHD, LBFP, MFE1, PBFE, FRTS3, L-PBE

Protein Name: peroxisomal bifunctional enzyme

Poids moléculaire: 79kDa

ID gène: 1962

NCBI Accession: NP_001957

UniProt: Q08426

Pathways: Monocarboxylic Acid Catabolic Process