PMS2 Antibody (YA1772),MedChemexpress,HY-P82027

PMS2 Antibody (YA1772) is a Mouse-derived and non-conjugated IgG2b monoclonal antibody, targeting to PMS2.

Host

Mouse

Reactivity

Human

Application

WB,IHC-P,ICC/IF

Conjugate

Non-conjugated

Platform ID

BAB448656940

Suppliers

(1)

Biomedical Life sciences

91-9676853503

Country:India
City:Madīnat Ḩamad
Plot No.A-2811121/A&B/3.IP NACHARAM. ALA NACHARAM, Road N0-15, Hyderabad Medchal Malkajgiri, Telangana-500076
Master of Bioactive Molecules

MedChemexpress

Master of Bioactive Molecules

Headquarters

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Contact

Tel: 609-228-6898
Fax: 609-228-5909

Product Specifications
Scientific Background
Synonyms

Specifications

NamePMS2 Antibody (YA1772)
Cat. No.HY-P82027
Accession NumberP54278
Gene ID (Entrez)5395
HostMouse
IsotypeIgG2b
SensitivityEndogenous
ReactivityHuman
ConjugationNon-conjugated
ApplicationWB,IHC-P,ICC/IF
Working DilutionsWB: 1:500-1:1000 IHC-P: 1:50-1:100 ICC/IF: 1:100-1:200
ClonalityMonoclonal
Clone NumberYA1772
Molecular WeightPredicted band size: 96 kDa; Observed band size: 150 kDa
ImmunogenFull length human recombinant protein of human PMS2 produced in 293T cell.
PurityAffinity Purified
Appearance/FormLiquid
ShippingShipping with blue ice.
FormulationLiquid in PBS containing 50% glycerol, 1% BSA and 0.02% sodium azide, pH 7.3.
StorageStored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
Regulatory StatusResearch Use Only

Scientific Background

The protein encoded by The related gene is a key component of the mismatch repair system that functions to correct DNA mismatches and small insertions and deletions that can occur during DNA replication and homologous recombination. The protein forms heterodimers with the related gene product of the mutL homolog 1 (MLH1) related gene to form the MutL-alpha heterodimer. The MutL-alpha heterodimer possesses an endonucleolytic activity that is activated following recognition of mismatches and insertion/deletion loops by the MutS-alpha and MutS-beta heterodimers, and is necessary for removal of the mismatched DNA. There is a DQHA(X)2E(X)4E motif found at the C-terminus of the protein encoded by The related gene that forms part of the active site of the nuclease. Mutations in The related gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC; also known as Lynch syndrome) and Turcot syndrome.

Synonyms

DNA mismatch repair gene; DNA mismatch repair protein PMS2; HNPCC4; PMS1 protein homolog 2

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