Recombinant Anti-ALAD antibody [EPR10268(B)] (ab151754)


  • Product name

    Anti-ALAD antibody [EPR10268(B)]
    See all ALAD primary antibodies
  • Description

    Rabbit monoclonal [EPR10268(B)] to ALAD
  • Host species

  • Tested applications

    Suitable for: WB, IHC-Pmore details
    Unsuitable for: ICC or IP
  • Species reactivity

    Reacts with: Human
  • Immunogen

    Synthetic peptide corresponding to residues in Human ALAD (P13716)

  • Positive control

    • Human red blood cells or fetal liver lysate, Human kidney tissue.
  • General notes

    Mouse, Rat: We have preliminary internal testing data to indicate this antibody may not react with these species. Please contact us for more information.

    Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMab® patents.

    This product is a recombinant rabbit monoclonal antibody.


  • Form

  • Storage instructions

    Shipped at 4°C. Store at -20°C. Stable for 12 months at -20°C.
  • Storage buffer

    Preservative: 0.01% Sodium azide
    Constituents: 9% PBS, 40% Glycerol, 0.05% BSA, 50% Tissue culture supernatant
  • Purity

    Tissue culture supernatant
  • Clonality

  • Clone number

  • Isotype

  • Research areas


Our Abpromise guarantee covers the use of ab151754 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
WB 1/1000 - 1/10000. Predicted molecular weight: 36 kDa.
IHC-P 1/50 - 1/1000. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
  • Application notes
    Is unsuitable for ICC or IP.
  • Target

    • Function

      Catalyzes an early step in the biosynthesis of tetrapyrroles. Binds two molecules of 5-aminolevulinate per subunit, each at a distinct site, and catalyzes their condensation to form porphobilinogen.
    • Pathway

      Porphyrin metabolism; protoporphyrin-IX biosynthesis; coproporphyrinogen-III from 5-aminolevulinate: step 1/4.
    • Involvement in disease

      Defects in ALAD are the cause of acute hepatic porphyria (AHP) [MIM:612740]. AHP is a form of porphyria. Porphyrias are inherited defects in the biosynthesis of heme, resulting in the accumulation and increased excretion of porphyrins or porphyrin precursors. They are classified as erythropoietic or hepatic, depending on whether the enzyme deficiency occurs in red blood cells or in the liver. AHP is characterized by attacks of gastrointestinal disturbances, abdominal colic, paralysis, and peripheral neuropathy. Most attacks are precipitated by drugs, alcohol, caloric deprivation, infections, or endocrine factors.
    • Sequence similarities

      Belongs to the ALADH family.
    • Information by UniProt
    • Database links

    • Alternative names

      • ALAD antibody
      • ALADH antibody
      • ALADR antibody
      • Aminolevulinate dehydratase antibody
      • Aminolevulinate, delta, dehydratase antibody
      • Delta aminolevulinic acid dehydratase antibody
      • Delta-aminolevulinic acid dehydratase antibody
      • HEM2_HUMAN antibody
      • Lv antibody
      • MGC5057 antibody
      • OTTMUSP00000009376 antibody
      • OTTMUSP00000009377 antibody
      • PBGS antibody
      • Porphobilinogen synthase antibody
      • RP11-10I9.1 antibody
      • RP24-189G18.9 antibody
      see all


    • All lanes : Anti-ALAD antibody [EPR10268(B)] (ab151754) at 1/1000 dilution

      Lane 1 : Red blood cell lysate
      Lane 2 : Fetal liver lysate

      Lysates/proteins at 10 µg per lane.

      All lanes : HRP labelled goat anti-rabbit at 1/2000 dilution

      Predicted band size: 36 kDa

    • Immunohistochemical analysis of paraffin embedded Human kidney tissue labelling ALAD with ab151754 at a 1/50 dilution.


    This product has been referenced in:

    • Maio N  et al. Dimeric ferrochelatase bridges ABCB7 and ABCB10 homodimers in an architecturally defined molecular complex required for heme biosynthesis. Haematologica N/A:N/A (2019). Read more (PubMed: 30765471) »
    • Vandekeere S  et al. Serine Synthesis via PHGDH Is Essential for Heme Production in Endothelial Cells. Cell Metab N/A:N/A (2018). Read more (PubMed: 30017355) »
    See all 2 Publications for this product

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