| 存储条件 |
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| Product Name | MTA2 [17A1] |
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| Antibody Type | Primary Antibodies |
| Antigen Alias | DKFZp686F2281 antibody Mata1l1 antibody Metastasis associated 1 family member 2 antibody Metastasis associated 1 like 1 antibody Metastasis associated gene 1 like 1 antibody Metastasis associated gene family member 2 antibody Metastasis associated protein 2 antibody Metastasis associated protein MTA 2 antibody Metastasis associated protein MTA2 antibody Metastasis-associated 1-like 1 antibody Metastasis-associated protein MTA2 antibody Mmta2 antibody MTA1 L1 protein antibody MTA1-L1 protein antibody MTA1L1 antibody MTA2 antibody MTA2_HUMAN antibody p53 target protein in deacetylase complex antibody PID antibody |
| Product description | This gene encodes a protein that has been identified as a component of NuRD, a nucleosome remodeling deacetylase complex identified in the nucleus of human cells. It shows a very broad expression pattern and is strongly expressed in many tissues. It may represent one member of a small gene family that encode different but related proteins involved either directly or indirectly in transcriptional regulation. Their indirect effects on transcriptional regulation may include chromatin remodeling. It is closely related to another member of this family, a protein that has been correlated with the metastatic potential of certain carcinomas. These two proteins are so closely related that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. One of the proteins known to be a target protein for this gene product is p53. Deacetylation of p53 is correlated with a loss of growth inhibition in transformed cells supporting a connection between these gene family members and metastasis. |
| Immunogen | Recombinant protein within N-terminal human MTA2. |
| Clonality | Monoclonal |
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| Isotype | IgG1 |
| Host Species | Mouse |
| Tested Applications | WBIHC-PFC |
| WB:1:500-1:2,000: IHC-P:1:500-1:1,000: FC:1:50-1:100: | |
| Species Reactivity | Human |
| Concentration | 2mg/mL |
| Alternative Names | DKFZp686F2281 antibody Mata1l1 antibody Metastasis associated 1 family member 2 antibody Metastasis associated 1 like 1 antibody Metastasis associated gene 1 like 1 antibody Metastasis associated gene family member 2 antibody Metastasis associated protein 2 antibody Metastasis associated protein MTA 2 antibody Metastasis associated protein MTA2 antibody Metastasis-associated 1-like 1 antibody Metastasis-associated protein MTA2 antibody Mmta2 antibody MTA1 L1 protein antibody MTA1-L1 protein antibody MTA1L1 antibody MTA2 antibody MTA2_HUMAN antibody p53 target protein in deacetylase complex antibody PID antibody |
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| Molecular Weight(MW) | 75 kDa |
| Cellular Localization | Nucleus. |
| SwissProt ID | O94776 |
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Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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).Application
Fig8: Flow cytometric analysis of MTA2 was done on MCF-7 cells. The cells were fixed, permeabilized and stained with the primary antibody (EM1901-34, 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 | K562, MCF-7, SH-SY5Y, Daudi, human colon carcinoma tissue, human skin tissue, human breast tissue, human breast carcinoma tissue, human gastric carcinoma tissue, human small intestine tissue. |
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| Application Notes | WB:1:500-1:2,000: IHC-P:1:500-1:1,000: 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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