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Rabbit anti-Human ALDH6A1 Polyclonal Antibody

The antibody against ALDH6A1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 326-535 of human ALDH6A1 (NP_005580.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

ADA-00480A

The antibody against ALDH6A1 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 326-535 of human ALDH6A1 (NP_005580.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, IF/ICC, ELISA.

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Specifications


Cat.No ADA-00480A ClonalityPolyclonal
Host SpeciesRabbitTarget NameALDH6A1
Target SynonymsMMSDH; MMSADHA; ALDH6A1FormLiquid
Species ReactivityHuman, Mouse, RatIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesMouse kidney, 22Rv1, A-431, HepG2, MCF7, Mouse liver, Rat spinal cord, SH-SY5YApplicationELISA, WB, IF/ICC

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 326-535 of human ALDH6A1 (NP_005580.1).Target SpeciesHuman
Uniprot IDQ02252Immunogen Sequence
Background Information
  • Uniprot Id

    Q02252

  • Target Species

    Human

  • Target Name

    ALDH6A1

  • Target Full Name

    Methylmalonate-semialdehyde/malonate-semialdehyde dehydrogenase [acylating], mitochondrial

  • Target Function

    Plays a role in valine and pyrimidine metabolism. Binds fatty acyl-CoA.

  • Target Involvement

    Methylmalonate semialdehyde dehydrogenase deficiency (MMSDHD)

  • Target Subcellular Location

    Mitochondrion.

  • Target Protein Families

    Aldehyde dehydrogenase family

  • Target Synonyms

    MMSDH; MMSADHA; ALDH6A1

  • Target 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.

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