PMS2 antibody (clone 4G4), anti-human
€435.00
In stock
SKU
AC-AT3358a
Catalog Number: AC-AT3358a
Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: E
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Size: 100 µg
Isotype: mouse IgG2a Kappa
Applications: E
Request Information AC-AT3358a">Request Information
Background:
This gene is one of the PMS2 gene family members found in clusters on chromosome 7. The product of this gene is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Mutations in this gene are associated with hereditary nonpolyposis colorectal cancer, Turcot syndrome, and are a cause of supratentorial primitive neuroectodermal tumors. Alternatively spliced transcript variants have been observed for this gene.
Other Names:
Mismatch repair endonuclease PMS2, 31--, DNA mismatch repair protein PMS2, PMS1 protein homolog 2, PMS2, PMSL2
Antigen Type:
Recombinant Protein
Gene Name: PMS2 (HGNC:9122)
Gene ID: 5395
NCBI Accession: NP_000526.1
Primary Accession: P54278
Other Accession: NM_000535
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
This gene is one of the PMS2 gene family members found in clusters on chromosome 7. The product of this gene is involved in DNA mismatch repair. It forms a heterodimer with MLH1 and this complex interacts with other complexes bound to mismatched bases. Mutations in this gene are associated with hereditary nonpolyposis colorectal cancer, Turcot syndrome, and are a cause of supratentorial primitive neuroectodermal tumors. Alternatively spliced transcript variants have been observed for this gene.
Other Names:
Mismatch repair endonuclease PMS2, 31--, DNA mismatch repair protein PMS2, PMS1 protein homolog 2, PMS2, PMSL2
Antigen Type:
Recombinant Protein
Gene Name: PMS2 (HGNC:9122)
Gene ID: 5395
NCBI Accession: NP_000526.1
Primary Accession: P54278
Other Accession: NM_000535
Format: Clear, colorless solution in phosphate buffered saline, pH 7.2 .
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