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| Product Name | MCM7 [15E1] |
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| Antibody Type | Primary Antibodies |
| Antigen Alias | CDABP0042 antibody CDC 47 antibody CDC47 antibody CDC47 homolog antibody Cdc47, S. cerevisiae, homolog of antibody DNA replication licensing factor MCM7 antibody Homolog of S. cerevisiae Cdc47 antibody MCM 2 antibody MCM 7 antibody MCM2 antibody MCM2, formerly antibody Mcm7 antibody MCM7 minichromosome maintenance deficient 7 antibody MCM7_HUMAN antibody Minichromosome Maintainence 7 antibody Minichromosome maintainence, S. cerevisiae, homolog of antibody Minichromosome maintenance complex component 7 antibody Minichromosome maintenance deficient 7 antibody Minichromosome maintenance protein 7 antibody P1.1 MCM3 antibody P1.1-MCM3 antibody P1CDC47 antibody P85MCM antibody PNAS 146 antibody PNAS146 antibody PPP1R104 antibody Protein phosphatase 1, regulatory subunit 104 antibody |
| Product description | Acts as component of the MCM2-7 complex (MCM complex) which is the putative replicative helicase essential for 'once per cell cycle' DNA replication initiation and elongation in eukaryotic cells. The active ATPase sites in the MCM2-7 ring are formed through the interaction surfaces of two neighboring subunits such that a critical structure of a conserved arginine finger motif is provided in trans relative to the ATP-binding site of the Walker A box of the adjacent subunit. The six ATPase active sites, however, are likely to contribute differentially to the complex helicase activity. Required for S-phase checkpoint activation upon UV-induced damage. Early fractionation of eukaryotic MCM proteins yielded a variety of dimeric, trimeric and tetrameric complexes with unclear biological significance. Specifically a MCM467 subcomplex is shown to have in vitro helicase activity which is inhibited by the MCM2 subunit. The MCM2-7 hexamer is the proposed physiological active complex. |
| Immunogen | Synthetic peptide within human aa 500-719. |
| Clonality | Monoclonal |
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| Isotype | IgG1 |
| Host Species | Mouse |
| Tested Applications | WBIHCFC |
| WB:1:500-1:2,000: IHC-P:1:50-1:200: FC:1:50-1:100: | |
| Species Reactivity | HumanRat |
| Concentration | 2mg/mL |
| Alternative Names | CDABP0042 antibody CDC 47 antibody CDC47 antibody CDC47 homolog antibody Cdc47 S. cerevisiae homolog of antibody DNA replication licensing factor MCM7 antibody Homolog of S. cerevisiae Cdc47 antibody MCM 2 antibody MCM 7 antibody MCM2 antibody MCM2 formerly antibody Mcm7 antibody MCM7 minichromosome maintenance deficient 7 antibody MCM7_HUMAN antibody Minichromosome Maintainence 7 antibody Minichromosome maintainence S. cerevisiae homolog of antibody Minichromosome maintenance complex component 7 antibody Minichromosome maintenance deficient 7 antibody Minichromosome maintenance protein 7 antibody P1.1 MCM3 antibody P1.1-MCM3 antibody P1CDC47 antibody P85MCM antibody PNAS 146 antibody PNAS146 antibody PPP1R104 antibody Protein phosphatase 1 regulatory subunit 104 antibody |
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| Molecular Weight(MW) | 81 kDa |
| Cellular Localization | Nucleus. |
| SwissProt ID | P33993 |
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Application
Fig1: Western blot analysis of MCM7 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 (EM1901-12, 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: HL-60 cell lysate Lane 2: 293 cell lysate Lane 3: PC-12 cell lysate Lane 4: K562 cell lysate
Application
Fig2: Immunohistochemical analysis of paraffin-embedded human tonsil tissue using anti-MCM7 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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 (EM1901-12, 1/100) 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 esophagus tissue using anti-MCM7 antibody. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) 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 (EM1901-12, 1/100) 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: Flow cytometric analysis of MCM7 was done on SH-SY5Y cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-12, 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 Control | HL-60 cell, 293 cell, PC-12 cell, K562 cell, human tonsil tissue, human esophagus tissue, SH-SY5Y cell. |
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| Application Notes | WB:1:500-1:2,000: IHC-P:1:50-1:200: FC:1:50-1:100: |
| Form | Liquid |
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| Storage Instructions | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
| Storage Buffer | 1*TBS (pH7.4), 1%BSA, 50%Glycerol. Preservative: 0.05% Sodium Azide. |
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