Anticorpi MLH1

35 prodotti

MLH1 è un gene codificato dal simbolo MLH1. Comunemente indicato anche come: DNA mismatch repair protein MutL protein homolog 1; COCA2. MLH1 ha una massa di 84.6kDa, una lunghezza di amminoacidi di 756, ed è implicato nella malattia: Hereditary non-polyposis colorectal cancer 2; Mismatch repair cancer syndrome; Muir-Torre syndrome; Endometrial cancer; Colorectal cancer.

Offriamo 35 anticorpi contro MLH1, allevati nel Coniglio e Topo, che sono adatti per WB, IHC, ELISA e ICC/IF con campioni derivati ​​da Umano, Topo e Ratto.

Informazioni su geni e proteine

Riepilogo UniProt
Heterodimerizes with PMS2 to form MutL alpha, a component of the post-replicative DNA mismatch repair system (MMR). DNA repair is initiated by MutS alpha (MSH2-MSH6) or MutS beta (MSH2-MSH3) binding to a dsDNA mismatch, then MutL alpha is recruited to the heteroduplex. Assembly of the MutL-MutS-heteroduplex ternary complex in presence of RFC and PCNA is sufficient to activate endonuclease activity of PMS2. It introduces single-strand breaks near the mismatch and thus generates new entry points for the exonuclease EXO1 to degrade the strand containing the mismatch. DNA methylation would prevent cleavage and therefore assure that only the newly mutated DNA strand is going to be corrected. MutL alpha (MLH1-PMS2) interacts physically with the clamp loader subunits of DNA polymerase III, suggesting that it may play a role to recruit the DNA polymerase III to the site of the MMR. Also implicated in DNA damage signaling, a process which induces cell cycle arrest and can lead to apoptosis in case of major DNA damages. Heterodimerizes with MLH3 to form MutL gamma which plays a role in meiosis.
Sommario di Entrez
The protein encoded by this gene can heterodimerize with mismatch repair endonuclease PMS2 to form MutL alpha, part of the DNA mismatch repair system. When MutL alpha is bound by MutS beta and some accessory proteins, the PMS2 subunit of MutL alpha introduces a single-strand break near DNA mismatches, providing an entry point for exonuclease degradation. The encoded protein is also involved in DNA damage signaling and can heterodimerize with DNA mismatch repair protein MLH3 to form MutL gamma, which is involved in meiosis. This gene was identified as a locus frequently mutated in hereditary nonpolyposis colon cancer (HNPCC).
Specificità del tessuto
Colon, lymphocytes, breast, lung, spleen, testis, prostate, thyroid, gall bladder and heart.
Coinvolgimento nella malattia
Hereditary non-polyposis colorectal cancer 2: An autosomal dominant disease associated with marked increase in cancer susceptibility. It is characterized by a familial predisposition to early-onset colorectal carcinoma (CRC) and extra-colonic tumors 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. Clinically, HNPCC is often divided into two subgroups. Type I is characterized by hereditary predisposition to colorectal cancer, a young age of onset, and carcinoma observed in the proximal colon. Type II is characterized by 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.

Mismatch repair cancer syndrome: An autosomal recessive, rare, childhood cancer predisposition syndrome encompassing a broad tumor spectrum. This includes hematological malignancies, central nervous system tumors, Lynch syndrome-associated malignancies such as colorectal tumors as well as multiple intestinal polyps, embryonic tumors and rhabdomyosarcoma. Multiple cafe-au-lait macules, a feature reminiscent of neurofibromatosis type 1, are often found as first manifestation of the underlying cancer. Areas of skin hypopigmentation have also been reported in MMRCS patients.

Muir-Torre syndrome: Rare autosomal dominant disorder characterized by sebaceous neoplasms and visceral malignancy.

Endometrial cancer: A malignancy of endometrium, the mucous lining of the uterus. Most endometrial cancers are adenocarcinomas, cancers that begin in cells that make and release mucus and other fluids.

Colorectal cancer: A complex disease characterized by malignant lesions arising from the inner wall of the large intestine (the colon) and the rectum. Genetic alterations are often associated with progression from premalignant lesion (adenoma) to invasive adenocarcinoma. Risk factors for cancer of the colon and rectum include colon polyps, long-standing ulcerative colitis, and genetic family history.
Somiglianze di sequenza
Belongs to the DNA mismatch repair MutL/HexB family.
Posizione cellulare
Nucleus. Chromosome.

Recruited to chromatin in a MCM9-dependent manner.
Immunohistochemistry - Anti-MutL Protein Homolog 1 Antibody (V0094) - Antibodies.com
(8)
Visualizza prodotto10µl Dimensione di prova
Western Blot - Anti-MLH1 Antibody [ARC53543] (A308155) - Antibodies.com
(5)
Visualizza prodottoKnockout convalidato
Western Blot - Anti-MLH1 Antibody (C13086) - Antibodies.com
(3)
Visualizza prodotto10µg Dimensione di prova
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Immunohistochemistry - Anti-MLH1 Antibody [MLH1/6467] - BSA and Azide free (A278489) - Antibodies.com
(3)
Visualizza prodottoAnticorpo ricombinante
Immunohistochemistry - Anti-MLH1 Antibody [MLH1/6284R] - BSA and Azide free (A278617) - Antibodies.com
(3)
Visualizza prodottoAnticorpo ricombinante
Immunohistochemistry - Anti-MLH1 Antibody [MLH1/6467] (A277901) - Antibodies.com
(3)
Visualizza prodottoAnticorpo ricombinante
Immunohistochemistry - Anti-MLH1 Antibody [MLH1/6284R] (A278029) - Antibodies.com
(3)
Visualizza prodottoAnticorpo ricombinante
Western Blot - Anti-MLH1 Antibody (A308154) - Antibodies.com
(2)
Validation Data - Anti-MLH1 Antibody [G409.1] (A304642)
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Visualizza prodottoAnticorpo ricombinante
SDS-PAGE - Anti-MLH1 Antibody [MLH1/6710] (A277711) - Antibodies.com
Immunohistochemistry - Anti-MLH1 Antibody [G168-728] (A249351) - Antibodies.com
Visualizza prodottoAnticorpo ricombinante
Immunohistochemistry - Anti-MLH1 Antibody [IHC409] (A324420) - Antibodies.com
SDS-PAGE - Anti-MLH1 Antibody [MLH1/1324] - BSA and Azide free (A252530) - Antibodies.com
SDS-PAGE - Anti-MLH1 Antibody [MLH1/1324] (A249350) - Antibodies.com
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Visualizza prodottoAnticorpo ricombinante
Immunohistochemistry - Anti-MLH1 Antibody [G168-728] - BSA and Azide free (A252531) - Antibodies.com
Visualizza prodottoAnticorpo ricombinante
SDS-PAGE - Anti-MLH1 Antibody [MLH1/6710] - BSA and Azide free (A278299) - Antibodies.com
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Visualizza prodottoAnticorpo ricombinante
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Visualizza prodottoAnticorpo ricombinante
Anti-MLH1 (S467) Antibody from Bioworld Technology (BS2418) - Antibodies.com
Western blot - MLH1 Antibody from Signalway Antibody (32046) - Antibodies.com
Anti-MLH1 Antibody from Bioworld Technology (MB0151) - Antibodies.com
(2)
Western blot - MLH1 Monoclonal Antibody from Signalway Antibody (27214) - Antibodies.com
MLH1 Antibody from Signalway Antibody (35518) - Antibodies.com

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