Anti-Cyclobutane Pyrimidine Dimers (CPDs) mAb (Clone TDM-2)

Catalog No:
CAC-NM-DND-001
$599.00

Cyclobutane pyrimidine dimer (CPD)-specific mAb TDM-2 was cloned by fusing mouse myeloma cells with splenocytes from BALB/c mice immunized with methylated BSA conjugated with UVC-irradiated calf thymus DNA.

TDM-2 binds CPDs in denatured DNA from all organisms from bacteria to human and is validated for ELISA and indirect immunofluorescence.

Catalog numbers beginning with "CAC" are antibodies from our exclusive Cosmo Bio Antibody Collection. Visit the CAC Antibody homepage to browse the collection list, organized by research topic.

Cyclobutane pyrimidine dimer (CPD)-specific mAb TDM-2 was cloned by fusing mouse myeloma cells with splenocytes from BALB/c mice immunized with methylated BSA conjugated with UVC-irradiated calf thymus DNA. TDM-2 binds CPDs in denatured DNA from all organisms from bacteria to human and is validated for ELISA and indirect immunofluorescence.

Background

DNA damage in cells exposed to ultraviolet (UV) radiation plays significant roles in cell-cycle arrest, activation of DNA repair, cell killing, mutation, and neoplastic transformation. The major types of DNA damage induced by UVB (280-315 nm, component of sunlight) and by UVC (200-280 nm) are cyclobutane pyrimidine dimers (CPDs) and (6-4) photoproducts (6-4PPs), which are formed between adjacent pyrimidine nucleotides on the same strand of DNA. Approximately 70-80% of UV-induced DNA damage is CPDs and the remainder is 6-4PPs and Dewar isomers of 6-4PPs. In normal human cells, these types of DNA lesions are repaired by the nucleotide excision repair system.

(19) have established monoclonal antibodies specific for CPDs and 6-4PPs. These antibodies enable quantitation of photoproducts in DNA purified from cultured cells or from the skin epidermis by ELISA and to visualize and measure photoproducts in DNA in cultured cells or the skin by indirect immunofluorescence (IIF). This technology will contribute to studies of molecular mechanisms of cellular responses to UV and DNA damage in many research fields including cancer research, photobiology, dermatology, ophthalmology, immunology, and cosmetology.

Reactivity

  • CPDs in single-stranded DNA
  • CPDs formed in every dipyrimidine sequence (TT, TC, CT and CC)
  • CPDs formed in oligonucleotides consisting of more than eight bases

Applications

  • Immunocytochemistry            1:1500
  • ELISA                                     1:1000

Source

The CPD-specific hybridoma (clone TDM-2) was established by fusion of mouse myeloma cells with splenocytes from BALB/c mice immunized with methylated BSA conjugated with UVC-irradiated calf thymus DNA. Hybridoma culture supernatant was collected and precipitated with ice-cold ammonium sulfate. After centrifugation, the pellet, dissolved in small volume of double-distilled water, was dialyzed against PBS and lyophilized.

Formulation

  • Lyophilate to be reconstituted in 100 ml of distilled water
  • Contains no preservative

Storage

  • Lyophilized form        -20°C
  • Reconstituted form     -20°C
  • Stable for at least 1 year; aliquot to avoid freezing and thawing
Documents & Links for Anti-Cyclobutane Pyrimidine Dimers (CPDs) mAb (Clone TDM-2)
Datasheet Anti CPDs mAb (Clone TDM-2) Datasheet

Documents & Links for Anti-Cyclobutane Pyrimidine Dimers (CPDs) mAb (Clone TDM-2)
Datasheet Anti CPDs mAb (Clone TDM-2) Datasheet

Citations for Anti-Cyclobutane Pyrimidine Dimers (CPDs) mAb (Clone TDM-2) – 48 Found
AKAP12 mediates PKA-induced phosphorylation of ATR to enhance nucleotide excision repair.
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Human in vitro skin organ culture as a model system for evaluating DNA repair.
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Participation of chromatin-remodeling proteins in the repair of ultraviolet-B-damaged DNA.
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Highly specific and sensitive method for measuring nucleotide excision repair kinetics of ultraviolet photoproducts in human cells.
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High-resolution characterization of CPD hotspot formation in human fibroblasts.
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The contribution of mitochondrial thymidylate synthesis in preventing the nuclear genome stress.
Nucleic Acids Res. 2014 Apr;42(8):4972-84. doi: 10.1093/nar/gku152. Epub 2014 Feb 21.  PubMed
HAG3, a Histone Acetyltransferase, Affects UV-B Responses by Negatively Regulating the Expression of DNA Repair Enzymes and Sunscreen Content in Arabidopsis thaliana.
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Silymarin: Friend or Foe of UV Exposed Keratinocytes?
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The DNA repair domain of human rpS3 protects against photoaging by removing cyclobutane pyrimidine dimers.
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Rat Model of Cockayne Syndrome Neurological Disease.
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