产品简要
公司名称 :
MyBioSource
产品类型 :
抗体
产品名称 :
MLH1抗体
目录 :
MBS9605077
规格 :
0.1毫升
价格 :
240美元
克隆性 :
多克隆
宿主 :
共轭标签 :
未共轭
反应物种 :
人类, 小鼠, 大鼠
应用 :
免疫印迹, 酶联免疫吸附测定, 免疫细胞化学, 酶免疫法
更多信息或购买 :
图像
图像 1 :
MyBioSource MBS9605077 图像 1
Western blot analysis of extracts from K562 cells, using MLH1 antibody.The lane on the left is treated with the antigen-specific peptide.
图像 2 :
MyBioSource MBS9605077 图像 2
MBS9605077 staining K562 by IF/ICC. The sample were fixed with PFA and permeabilized in 0.1% Triton X-100, then blocked in 10% serum for 45 minutes at 25 degree C. The primary antibody was diluted at 1/200 and incubated with the sample for 1 hour at 37 degree C. An Alexa Fluor 594 conjugated goat anti-rabbit IgG (H+L) Ab, diluted at 1/600, was used as the secondary antibody.
图像 3 :
MyBioSource MBS9605077 图像 3
Western blot analysis of extracts from mouse lung, using MLH1 Antibody.
产品信息
目录号 :
MBS9605077
产品类型 :
抗体
产品全称 :
MLH1抗体
产品简称 :
[MLH1]
其他名称 :
[DNA mismatch repair protein Mlh1 isoform 1; DNA mismatch repair protein Mlh1; DNA mismatch repair protein Mlh1; mutL homolog 1; MutL protein homolog 1]
产品基因名称 :
[MLH1]
其他基因名称 :
[MLH1;MLH1;FCC2;COCA2;HNPCC;hMLH1;HNPCC2;COCA2]
克隆性 :
多克隆
抗体亚型 :
IgG
宿主 :
反应物种 :
人类, 小鼠, 大鼠
序列长度 :
756
特异性 :
MLH1抗体检测内生水平总数MLH1
纯度 :
The antiserum was purified by peptide affinity chromatography using SulfoLink Coupling Resin.
形式 :
磷酸盐缓冲液, pH值7.4, 150mM氯化钠, 0.02% 叠氮化钠和50% 甘油
浓度 :
1毫克/毫升
储存稳定性 :
Store at -20 degree C. Stable for 12 months from date of receipt.
检测过的应用 :
免疫印迹(免疫印迹), 免疫荧光(IF), 免疫细胞化学(免疫细胞化学), 酶联免疫吸附测定(EIA)
应用笔记 :
WB: 1:500-1:1000. IF/ICC: 1:100-1:500. IMPORTANT: For western blots, incubate membrane with diluted Ab in 5% w/v milk, 1 x TBS, 0.1% Tween 20 at 4°C with gentle shaking, overnight.
image1头 :
免疫印迹(免疫印迹)
image2头 :
Immunofluorescene (IF)
image3头 :
免疫印迹(免疫印迹)
其它信息1 :
Immunogen: A synthesized peptide derived from human MLH1, corresponding to a region within the internal amino acids.
产品描述 :
Function: 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-MSH6) 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. Similarity: Belongs to the DNA mismatch repair MutL/HexB family.
NCBI GI登录号 :
4557757
NCBI登录号 :
NP_000240.1
NCBI基因登录号 :
NM_000249.3
UniProt数据库登录号 :
P40692
NCBI分子量 :
85 KD
NCBI信号通路 :
BRCA1-associated Genome Surveillance Complex (BASC) Pathway (413428); Colorectal Cancer Pathway (83106); Colorectal Cancer Pathway (518); Direct P53 Effectors Pathway (137939); Endometrial Cancer Pathway (83109); Endometrial Cancer Pathway (521); Fanconi Anemia Pathway (377262); Fanconi Anemia Pathway (377128); Meiosis Pathway (477133); Meiotic Recombination Pathway (205242)
NCBI总结 :
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). [provided by RefSeq, Aug 2017]
UniProt数据库总结 :
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.
尺寸1 :
0.1毫升
价格1 :
240美元
尺寸2 :
0.2毫升
价格2 :
280
更多信息或购买 :
公司信息
MyBioSource
P.O. Box 153308
San Diego, CA 92195-3308
sales@mybiosource.com
https://www.mybiosource.com
1-858-633-0165
公司总部: 美国
MyBioSource,LLC最初由三名热情澎湃的提供高品质试剂的科学家联合创立于温哥华,公司愿景是“生物研究试剂的源头”,现在位于圣地亚哥市。