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MABE324 Anti-MSH3 Antibody, clone 1F6

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MABE324
100 µg  
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Overview

Replacement Information

Key Specifications Table

Species ReactivityKey ApplicationsHostFormatAntibody Type
MWB, ICCMPurifiedMonoclonal Antibody
Description
Catalogue NumberMABE324
DescriptionAnti-MSH3 Antibody, clone 1F6
Alternate Names
  • DNA mismatch repair protein Msh3
  • Protein repair-1
  • REP-1
  • Protein repair-3
  • REP-3
Background InformationMSH3, also known as DNA mismatch repair protein Msh3, Protein repair-1, REP-1, or Protein repair-3, REP-3, and encoded by the gene MSH3/REP-3, is an important component of the post-replicative DNA mismatch repair system. MSH3 heterodimerizes with MSH2 to form a complex named MutS beta which binds DNA mismatches and initiates DNA repair. MSH3/MSH2 complex (MutS beta) also complexes with another protein complex called MutL alpha which is also necessary for further steps in DNA repair. MSH3 is also frequently mutated in many cancers resulting in a mismatch repair deficiency and this can contribute to sensitivity to cytotoxic drugs. Interestingly too, because MSH3 is involved in DNA repair, it appears to it can mediate sensitivity to various repeat-associated diseases such as Huntington’s disease.
References
Product Information
FormatPurified
PresentationPurified mouse monoclonal IgG1κ in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.
Quality LevelMQ100
Applications
ApplicationThis Anti-MSH3 Antibody, clone 1F6 is validated for use in Western Blotting and Immunocytochemistry for the detection of MSH3.
Key Applications
  • Western Blotting
  • Immunocytochemistry
Application NotesWestern Blotting Analysis: 0.5 µg/mL of this antibody detected MSH3 in 10 µg of mouse testis tissue lysate.

Immunocytochemistry Analysis: A representative lot detected MSH3 in C2C12 cells (Prof. Glenn Morris, Wolfson Centre for Inherited Neuromuscular Disease.; Holt, I., et al. (2011). J Cell Biochem. 112(6):1612-1621.).
Biological Information
ImmunogenRecombinant protein corresponding to mouse MSH3.
Clone1F6
Concentration1 mg/mL
HostMouse
IsotypeIgG1κ
Species Reactivity
  • Mouse
Antibody TypeMonoclonal Antibody
Entrez Gene Number
Gene Symbol
  • Msh3
  • Rep-3
Purification MethodProtein G Purified
UniProt Number
Molecular Weight~123 kDa observed
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Quality AssuranceEvaluated by Western Blotting in C2C12 cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected MSH3 in 10 µg of C2C12 cell lysate.
Usage Statement
  • 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.
Storage and Shipping Information
Storage ConditionsStable for 1 year at 2-8°C from date of receipt.
Packaging Information
Material Size100 µg
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalog Number GTIN
MABE324 04053252977640

Documentation

Anti-MSH3 Antibody, clone 1F6 SDS

Title

Safety Data Sheet (SDS) 

Anti-MSH3 Antibody, clone 1F6 Certificates of Analysis

TitleLot Number
Anti-MSH3, clone 1F6 - Q2433685 Q2433685
Anti-MSH3, clone 1F6 - 3303104 3303104
Anti-MSH3, clone 1F6 - 3532434 3532434
Anti-MSH3, clone 1F6 - 3807984 3807984
Anti-MSH3, clone 1F6 - 3923735 3923735
Anti-MSH3, clone 1F6 - 3957849 3957849
Anti-MSH3, clone 1F6 - 4080486 4080486
Anti-MSH3, clone 1F6 - 4126093 4126093
Anti-MSH3, clone 1F6 - 4152520 4152520
Anti-MSH3, clone 1F6 - 4161507 4161507

References

Reference overviewPub Med ID
The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress.
Holt, Ian, et al.
J. Cell. Biochem., 112: 1612-21 (2011)  2011

Show Abstract
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