PMS2 antibody (AA 390-670)

Catalog No. ABIN6145829

Product Details anti-PMS2 Antibody

Target: PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

Binding Specificity: AA 390-670

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This PMS2 antibody is un-conjugated

Application: Western Blotting (WB)

Sequence: ADLEKPMVEK QDQSPSLRTG EEKKDVSISR LREAFSLRHT TENKPHSPKT PEPRRSPLGQ KRGMLSSSTS GAISDKGVLR PQKEAVSSSH GPSDPTDRAE VEKDSGHGST SVDSEGFSIP DTGSHCSSEY AASSPGDRGS QEHVDSQEKA PKTDDSFSDV DCHSNQEDTG CKFRVLPQPT NLATPNTKRF KKEEILSSSD ICQKLVNTQD MSASQVDVAV KINKKVVPLD FSMSSLAKRI KQLHHEAQQS EGEQNYRKFR AKICPGENQA AEDELRKEIS K

Cross-Reactivity: Human, Rat

Characteristics: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 390-670 of human PMS2 (NP_000526.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for PMS2

Target: PMS2 (PMS2 Postmeiotic Segregation Increased 2 (S. Cerevisiae) (PMS2))

Alternative Name: PMS2 (PMS2 Products)

Background: The protein encoded by this 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. This protein forms heterodimers with the gene product of the mutL homolog 1 (MLH1) 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 this gene that forms part of the active site of the nuclease. Mutations in this gene have been associated with hereditary nonpolyposis colorectal cancer (HNPCC, also known as Lynch syndrome) and Turcot syndrome.,PMS2,HNPCC4,MLH4,PMS2CL,PMSL2,PMS2

Molecular Weight: 20 kDa/51 kDa/62 kDa/95 kDa

Gene ID: 5395

UniProt: P54278

Pathways: DNA Damage Repair, Production of Molecular Mediator of Immune Response