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ALDH6A1 antibody (AA 1-195)

This Mouse Monoclonal antibody specifically detects ALDH6A1 in WB, ELISA, IHC, FACS and ICC. It exhibits reactivity toward Human.
Catalog No. ABIN5542265

Quick Overview for ALDH6A1 antibody (AA 1-195) (ABIN5542265)

Target

See all ALDH6A1 Antibodies
ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

Reactivity

  • 59
  • 10
  • 8
  • 3
  • 3
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 46
  • 10
  • 3
Mouse

Clonality

  • 51
  • 8
Monoclonal

Conjugate

  • 33
  • 5
  • 5
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This ALDH6A1 antibody is un-conjugated

Application

  • 47
  • 35
  • 30
  • 11
  • 9
  • 5
  • 5
  • 2
  • 1
Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Flow Cytometry (FACS), Immunocytochemistry (ICC)

Clone

6H9B8
  • Binding Specificity

    • 9
    • 8
    • 7
    • 6
    • 4
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-195

    Purpose

    ALDH6A1 Antibody

    Purification

    Purified antibody

    Immunogen

    Purified recombinant fragment of human ALDH6A1 (AA: 1-195) expressed in E. Coli.

    Isotype

    IgG1
  • Application Notes

    ELISA: 1/10000

    FCM: 1/200 - 1/400

    ICC: 1/200 - 1/1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified antibody in PBS with 0.05 % 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.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
  • Target

    ALDH6A1 (Aldehyde Dehydrogenase 6 Family, Member A1 (ALDH6A1))

    Alternative Name

    ALDH6A1

    Background

    This gene encodes a member of the aldehyde dehydrogenase protein family. The encoded protein is a mitochondrial methylmalonate semialdehyde dehydrogenase that plays a role in the valine and pyrimidine catabolic pathways. This protein catalyzes the irreversible oxidative decarboxylation of malonate and methylmalonate semialdehydes to acetyl- and propionyl-CoA. Methylmalonate semialdehyde dehydrogenase deficiency is characterized by elevated beta-alanine, 3-hydroxypropionic acid, and both isomers of 3-amino and 3-hydroxyisobutyric acids in urine organic acids. Alternate splicing results in multiple transcript variants.

    Molecular Weight

    57.8 kDa

    Gene ID

    4329

    UniProt

    Q02252

    Pathways

    Brown Fat Cell Differentiation
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