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MLH3 blocking peptide

MLH3 Immunizing Peptide

Gene Names
MLH3; HNPCC7
Reactivity
Human, Dog, Pig
Synonyms
MLH3; MLH3 Immunizing Peptide; mutL homolog 3 (E. coli); HNPCC; HNPCC7; MGC138372; S240II117; mutL (E. coli) homolog 3; mismatch repair gene MLH3; DNA mismatch repair protein MLH3; mutL homolog 3; MLH3 blocking peptide
Ordering
For Research Use Only!
Reactivity
Human, Dog, Pig
Form/Format
100ug of dried peptide
Sequence
RQSLQQSMPPCEPP
Sequence Length
1453
Preparation and Storage
Shipped at ambient temperature, store at -20 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
Molecular Weight
161,021 Da
NCBI Official Full Name
DNA mismatch repair protein Mlh3 isoform 1
NCBI Official Synonym Full Names
mutL homolog 3
NCBI Official Symbol
MLH3
NCBI Official Synonym Symbols
HNPCC7
NCBI Protein Information
DNA mismatch repair protein Mlh3
UniProt Protein Name
DNA mismatch repair protein Mlh3
UniProt Gene Name
MLH3
UniProt Entry Name
MLH3_HUMAN

NCBI Description

This gene is a member of the MutL-homolog (MLH) family of DNA mismatch repair (MMR) genes. MLH genes are implicated in maintaining genomic integrity during DNA replication and after meiotic recombination. The protein encoded by this gene functions as a heterodimer with other family members. Somatic mutations in this gene frequently occur in tumors exhibiting microsatellite instability, and germline mutations have been linked to hereditary nonpolyposis colorectal cancer type 7 (HNPCC7). Several alternatively spliced transcript variants have been identified, but the full-length nature of only two transcript variants has been determined. [provided by RefSeq, Jul 2008]

Uniprot Description

MLH3: Probably involved in the repair of mismatches in DNA. Defects in MLH3 are the cause of hereditary non-polyposis colorectal cancer type 7 (HNPCC7). Mutations in more than one gene locus can be involved alone or in combination in the production of the HNPCC phenotype (also called Lynch syndrome). Most families with clinically recognized HNPCC have mutations in either MLH1 or MSH2 genes. HNPCC is an autosomal, dominantly inherited disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early onset colorectal carcinoma (CRC) and extra-colonic cancers of the gastrointestinal, urological and female reproductive tracts. HNPCC is reported to be the most common form of inherited colorectal cancer in the Western world, and accounts for 15% of all colon cancers. Cancers in HNPCC originate within benign neoplastic polyps termed adenomas. Clinically, HNPCC is often divided into two subgroups. Type I: hereditary predisposition to colorectal cancer, a young age of onset, and carcinoma observed in the proximal colon. Type II: patients have an increased risk for cancers in certain tissues such as the uterus, ovary, breast, stomach, small intestine, skin, and larynx in addition to the colon. Diagnosis of classical HNPCC is based on the Amsterdam criteria: 3 or more relatives affected by colorectal cancer, one a first degree relative of the other two; 2 or more generation affected; 1 or more colorectal cancers presenting before 50 years of age; exclusion of hereditary polyposis syndromes. The term 'suspected HNPCC' or 'incomplete HNPCC' can be used to describe families who do not or only partially fulfill the Amsterdam criteria, but in whom a genetic basis for colon cancer is strongly suspected. Defects in MLH3 are a cause of colorectal cancer (CRC). Belongs to the DNA mismatch repair MutL/HexB family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: DNA repair, damage; Cell cycle regulation

Chromosomal Location of Human Ortholog: 14q24.3

Cellular Component: chiasma; male germ cell nucleus; nucleus; synaptonemal complex

Molecular Function: ATP binding; ATPase activity; centromeric DNA binding; chromatin binding; mismatched DNA binding; protein binding; satellite DNA binding; single-stranded DNA binding

Biological Process: female meiosis I; male meiosis; meiotic recombination; mismatch repair; protein localization; synaptonemal complex assembly

Disease: Colorectal Cancer, Hereditary Nonpolyposis, Type 7; Endometrial Cancer

Research Articles on MLH3

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Product Notes

The MLH3 mlh3 (Catalog #AAA425817) is a Blocking Peptide and is intended for research purposes only. The product is available for immediate purchase. The MLH3 Immunizing Peptide reacts with Human, Dog, Pig and may cross-react with other species as described in the data sheet. The amino acid sequence is listed below: RQSLQQSMPP CEPP. It is sometimes possible for the material contained within the vial of "MLH3, Blocking Peptide" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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