• Product nameAnti-MLH3 antibody
    See all MLH3 primary antibodies
  • Description
    Rabbit polyclonal to MLH3
  • Tested applicationsSuitable for: WBmore details
  • Species reactivity
    Reacts with: Human
    Predicted to work with: Mouse, Rat
  • Immunogen

    Recombinant fragment, corresponding to a region within amino acids 1-282 of Human MLH3 (AAI12168).

  • Positive control
    • A549, HeLa, HepG2 and HCT116 whole cell lysates.


  • FormLiquid
  • Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
  • Storage bufferpH: 7.00
    Preservative: 0.01% Thimerosal (merthiolate)
    Constituents: 20% Glycerol, 1.21% Tris, 0.75% Glycine
  • Concentration information loading...
  • PurityImmunogen affinity purified
  • Purification notesab111942 is purified by antigen-affinity chromatography.
  • ClonalityPolyclonal
  • IsotypeIgG
  • Research areas


Our Abpromise guarantee covers the use of ab111942 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 1/500 - 1/3000. Predicted molecular weight: 161 kDa.


  • FunctionProbably involved in the repair of mismatches in DNA.
  • Tissue specificityUbiquitous.
  • Involvement in diseaseDefects in MLH3 are the cause of hereditary non-polyposis colorectal cancer type 7 (HNPCC7) [MIM:614385]. Mutations in more than one gene locus can be involved alone or in combination in the production of the HNPCC phenotype (also called Lynch syndrome). Most families with clinically recognized HNPCC have mutations in either MLH1 or MSH2 genes. HNPCC is an autosomal, dominantly inherited disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early onset colorectal carcinoma (CRC) and extra-colonic cancers of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the Western world, and accounts for 15% of all colon cancers. Cancers in HNPCC originate within benign neoplastic polyps termed adenomas. Clinically, HNPCC is often divided into two subgroups. Type I: hereditary predisposition to colorectal cancer, a young age of onset, and carcinoma observed in the proximal colon. Type II: patients have an increased risk for cancers in certain tissues such as the uterus, ovary, breast, stomach, small intestine, skin, and larynx in addition to the colon. Diagnosis of classical HNPCC is based on the Amsterdam criteria: 3 or more relatives affected by colorectal cancer, one a first degree relative of the other two; 2 or more generation affected; 1 or more colorectal cancers presenting before 50 years of age; exclusion of hereditary polyposis syndromes. The term 'suspected HNPCC' or 'incomplete HNPCC' can be used to describe families who do not or only partially fulfill the Amsterdam criteria, but in whom a genetic basis for colon cancer is strongly suspected.
    Defects in MLH3 are a cause of colorectal cancer (CRC) [MIM:114500].
  • Sequence similaritiesBelongs to the DNA mismatch repair mutL/hexB family.
  • Cellular localizationNucleus.
  • Information by UniProt
  • Database links
  • Alternative names
    • DNA mismatch repair protein Mlh3 antibody
    • HNPCC 7 antibody
    • HNPCC antibody
    • HNPCC7 antibody
    • MGC138372 antibody
    • Mismatch repair gene MLH 3 antibody
    • Mismatch repair gene MLH3 antibody
    • MLH 3 antibody
    • MLH3 antibody
    • MLH3_HUMAN antibody
    • MutL homolog 3 (E. coli) antibody
    • MutL homolog 3 antibody
    • MutL protein homolog 3 antibody
    • S240II117 antibody
    see all

Anti-MLH3 antibody images

  • Anti-MLH3 antibody (ab111942) at 1/1000 dilution + HCT116 whole cell lysate at 30 µg

    Predicted band size : 161 kDa

References for Anti-MLH3 antibody (ab111942)

ab111942 has not yet been referenced specifically in any publications.

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