ALDH3B1 anticorps (C-Term)

N° du produit ABIN360239

L’anticorps anti-ALDH3B1 Polyclonal Lapin est utilisé pour la détection de ALDH3B1 dans des échantillons de Humain. Il a été validé pour WB, IHC (p) et EIA.

Aperçu rapide pour ALDH3B1 anticorps (C-Term) (ABIN360239)

Antigène: ALDH3B1 (Aldehyde Dehydrogenase 3 Family, Member B1 (ALDH3B1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ALDH3B1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-ALDH3B1 anticorps

Épitope: C-Term

Specificité: This antibody reacts to ALDH4A1.

Purification: Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS

Immunogène: This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human ALDH4A1.

Isotype: Ig Fraction

Information d'application

Indications d'application: ELISA: 1/1,000. Western blotting: 1/50 - 1/100. Immunohistochemistry: 1/50 - 1/100.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: PBS with 0.09 % (W/V) sodium azide

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 freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.

Détails sur ALDH3B1

Antigène: ALDH3B1 (Aldehyde Dehydrogenase 3 Family, Member B1 (ALDH3B1))

Autre désignation: ALDH4

Sujet: ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.Synonyms: ALDH4A1, Aldehyde dehydrogenase family 4 member A1, Delta-1-pyrroline-5-carboxylate dehydrogenase mitochondrial, P5C dehydrogenase, P5CDH

ID gène: 8659, 9606

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process