ALDH3B1 antibody (C-Term)

Catalog No. ABIN360239

The Rabbit Polyclonal anti-ALDH3B1 antibody is suitable to detect ALDH3B1 in samples from Human. It has been validated for WB, IHC (p) and EIA.

Quick Overview for ALDH3B1 antibody (C-Term) (ABIN360239)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ALDH3B1 antibody is un-conjugated

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

Product Details anti-ALDH3B1 Antibody

Binding Specificity: C-Term

Specificity: This antibody reacts to ALDH4A1.

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

Immunogen: 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

Application Details

Application Notes: 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

Handling

Format: Liquid

Concentration: 0.25 mg/mL

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

Preservative: Sodium azide

Precaution of Use: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

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

Target Details for ALDH3B1

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

Alternative Name: ALDH4

Background: 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

Gene ID: 8659, 9606

UniProt: P30038

Pathways: Monocarboxylic Acid Catabolic Process