ALDH3B1
Reactivité: Humain
WB
Hôte: Lapin
Polyclonal
unconjugated
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
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.
Antigène
ALDH3B1
(Aldehyde Dehydrogenase 3 Family, Member B1 (ALDH3B1))
anticorps ALDH4, anticorps ALDH7, anticorps aldh4, anticorps aldh7, anticorps 1700001N19Rik, anticorps aldh3d1, anticorps cb508, anticorps fb17d04, anticorps wu:fb17d04, anticorps aldehyde dehydrogenase 3 family member B1, anticorps aldehyde dehydrogenase 3 family member B1 L homeolog, anticorps aldehyde dehydrogenase 3 family, member B1, anticorps aldehyde dehydrogenase family 3 member B1, anticorps ALDH3B1, anticorps aldh3b1.L, anticorps Aldh3b1, anticorps LOC100548954, anticorps aldh3b1
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