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MGST1 [14H2]

MGST1 [14H2]

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100ul 现货2-3天 原装正品
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基础信息
存储条件
产品详情
Product Profile
Product NameMGST1 [14H2]
Antibody TypePrimary Antibodies
Product descriptionThe MAPEG (Membrane Associated Proteins in Eicosanoid and Glutathione metabolism) family consists of six human proteins, two of which are involved in the production of leukotrienes and prostaglandin E, important mediators of inflammation. Other family members, demonstrating glutathione S-transferase and peroxidase activities, are involved in cellular defense against toxic, carcinogenic, and pharmacologically active electrophilic compounds. This gene encodes a protein that catalyzes the conjugation of glutathione to electrophiles and the reduction of lipid hydroperoxides. This protein is localized to the endoplasmic reticulum and outer mitochondrial membrane where it is thought to protect these membranes from oxidative stress. Several transcript variants, some non-protein coding and some protein coding, have been found for this gene.
ImmunogenSynthetic peptide within human aa 1-130.
Key Feature
ClonalityMonoclonal
IsotypeIgG1
Host SpeciesMouse
Tested ApplicationsWB,IHC,FC

WB:1:500-1:2,000IHC-P:1:100-1:200FC:1:50-1:100
Species ReactivityHuman,Mouse,Rat
Concentration2mg/mL
PurificationUnpurified
Target Information
Alternative NamesMGST1 antibody Glutathione S transferase 12 antibody GST12 antibody MGST 1 antibody MGST antibody MGST I antibody MGST1 antibody MGST1_HUMAN antibody Microsomal glutathione S-transferase 1 antibody Microsomal GST 1 antibody Microsomal GST-1 antibody Microsomal GST-I antibody
Molecular Weight(MW)18 kDa
Cellular LocalizationEndoplasmic reticulum, Mitochondrion.
Database Links
SwissProt IDP10620Q91VS7P08011
Application

Application

Fig1: Western blot analysis of MGST1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (EM1901-13, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: SiHa cell lysate Lane 2: HepG2 cell lysate Lane 3: A549 cell lysate Lane 4: U937 cell lysate

Application

Fig2: Immunohistochemical analysis of paraffin-embedded rat kidney tissue using anti-MGST1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1901-13, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Application

Fig3: Immunohistochemical analysis of paraffin-embedded human liver carcinoma tissue using anti-MGST1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1901-13, 1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Application

Fig4: Immunohistochemical analysis of paraffin-embedded human colon tissue using anti-MGST1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1901-13, 1/200) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Application

Fig5: Immunohistochemical analysis of paraffin-embedded human placenta tissue using anti-MGST1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1901-13, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Application

Fig6: Immunohistochemical analysis of paraffin-embedded mouse liver tissue using anti-MGST1 antibody. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 8.0-8.4) for 20 minutes.The tissues were blocked in 5% BSA for 30 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (EM1901-13, 1/50) for 30 minutes at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

Application

Fig7: Flow cytometric analysis of MGST1 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-13, 1/50) (red). After incubation of the primary antibody at room temperature for an hour, the cells were stained with a Alexa Fluor 488-conjugated Goat anti-Mouse IgG Secondary antibody at 1/1000 dilution for 30 minutes.Unlabelled sample was used as a control (cells without incubation with primary antibody; black).
Positive ControlSiHa cell, HepG2 cell, A549 cell, U937 cell, rat kidney tissue, human liver carcinoma tissue, human colon tissue, human placenta tissue, mouse liver tissue, MCF-7 cell.
Application NotesWB:1:500-1:2,000IHC-P:1:100-1:200FC:1:50-1:100
Additional Information
FormLiquid
Storage InstructionsStore at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles.
Storage Buffer1*TBS (pH7.4), 1%BSA, 50%Glycerol. Preservative: 0.05% Sodium Azide.


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