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MABC1040

Sigma-Aldrich

Anti-MTH1 Antibody, clone 11A3.2

clone 11A3.2, from mouse

Synonym(s):

7,8-dihydro-8-oxoguanine triphosphatase, 2-hydroxy-dATP diphosphatase, 8-oxo-dGTPase, Nucleoside diphosphate-linked moiety X motif 1, Nudix motif 1

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

11A3.2, monoclonal

species reactivity

human

technique(s)

western blot: suitable

isotype

IgG1κ

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... NUDT1(4521)

General description

7,8-dihydro-8-oxoguanine triphosphatase (EC 3.6.1.55; UniProt P36639; also known as 2-hydroxy-dATP diphosphatase, 8-oxo-dGTPase, Nucleoside diphosphate-linked moiety X motif 1, Nudix motif 1) is encoded by the NUDT1 (also known as MTH1) gene (Gene ID 4521) in human. Human MTH1/NUDT1 is the bacterial mutT ortholog that functions as a nucleotide pool-sanitising enzyme. MTH1/NUDT1 cleaves oxidized nucleotides such as 8-oxo-deoxyguanosinetri-phosphate (8-oxo-dGTP) and converts the triphosphates into the corresponding mono-phosphates. The hydrolysis reaction assures that the oxidized nucleotides can no longer be recognized by DNA polymerase, thereby preventing bases mispairing and transversion mutations by avoiding their incorporation during DNA replication. Upregulated MTH1 levels are found in cancer cells as a means to reduce 8-oxo-dGTP accumulation in the nucleotide pool due to high oxidative stress levels in these cells.

Specificity

Clone 11A3.2 recognizes an epitope present in all four spliced isoforms of human NUDT1/MTH1 reported by UniProt (P36639).

Immunogen

Epitope: C-terminal half.
GST-tagged recombinant human MTH1 C-terminal fragment.

Application

Anti-MTH1 Antibody, clone 11A3.2 is an antibody against MTH1 for use in Western Blotting.
Research Category
Apoptosis & Cancer
Research Sub Category
Apoptosis - Additional

Quality

Evaluated by Western Blotting in Jurkat cell lysate.

Western Blotting Analysis: 1.0 µg/mL of this antibody detected MTH1 in 10 µg of Jurkat cell lysate.

Target description

~20 kDa observed. 22.52 kDa (isoform p26), 20.30 kDa (isoform p22), 19.47 kDa (isoform p21), 17.95 kDa (isoform p18) calculated. Uncharacterized band(s) may appear in some lysates.

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Storage and Stability

Stable for 1 year at 2-8°C from date of receipt.

Other Notes

Concentration: Please refer to lot specific datasheet.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

MABC1040:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Patrick J Shilling et al.
Communications biology, 3(1), 214-214 (2020-05-10)
The pET series of expression plasmids are widely used for recombinant protein production in Escherichia coli. The genetic modules controlling transcription and translation in these plasmids were first described in the 1980s and have not changed since. Herein we report

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