Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human, Mouse, Rat |
Applications: | WB, IF-Cell, IF-Tissue, IHC-P, IP |
Clonality: | Monoclonal |
Clone number: | SZ17-01 |
Form: | Liquid |
Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term. |
Storage buffer: | 1*TBS (pH7.4), 0.05% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 55 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human ATF2 aa 456-505 / 505. |
Positive control: | HeLa cell lysate, 293T cell lysate, THP-1 cell lysate, mouse brain tissue lysate, rat brain tissue lysate, RAW264.7 cell lysate, SW480, Hela, MCF-7, PC-12, human breast carcinoma tissue. |
Subcellular location: | Nucleus, Membrane, Cytoplasm, Mitochondrion, Mitochondrion outer membrane. |
Recommended Dilutions:
WB IF-Cell IF-Tissue IHC-P IP |
1:1,000 1:50-1:200 1:50-1:200 1:200 Use at an assay dependent concentration. |
Uniprot #: | SwissProt: P15336 Human | P16951 Mouse | Q00969 Rat |
Alternative names: | Activating transcription factor 2 Activating transcription factor 2 splice variant ATF2 var2 ATF 2 Atf-2 Atf2 ATF2 protein ATF2_HUMAN cAMP Response Element Binding Protein 2 cAMP response element binding protein CRE BP1 cAMP response element-binding protein CRE-BP1 cAMP responsive element binding protein 2, formerly cAMP-dependent transcription factor ATF-2 cAMP-responsive element-binding protein 2 CRE BP1 CRE-BP CREB 2 CREB-2 CREB2 CREBP1 Cyclic AMP dependent transcription factor ATF 2 Cyclic AMP-dependent transcription factor ATF-2 Cyclic AMP-responsive element-binding protein 2 D130078H02Rik D18875 HB 16 HB16 Histone acetyltransferase ATF2 MGC105211 MGC105222 MGC111558 MGC142504 mXBP MXBP protein Tg(Gzma-Klra1)7Wum TREB 7 TREB7 |
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Fig1:
Western blot analysis of ATF2 on different lysates with Rabbit anti-ATF2 antibody (ET1603-15) at 1/1,000 dilution. Lane 1: HeLa cell lysate Lane 2: 293T cell lysate Lane 3: THP-1 cell lysate Lane 4: Mouse brain tissue lysate Lane 5: Rat brain tissue lysate Lane 6: RAW264.7 cell lysate Lysates/proteins at 30 µg/Lane. Predicted band size: 55 kDa Observed band size: 70 kDa Exposure time: 1 minute; ECL: K1801; 4-20% SDS-PAGE gel. Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (ET1603-15) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2: ICC staining of ATF2 in SW480 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1603-15, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |
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Fig3: ICC staining of ATF2 in Hela cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1603-15, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |
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Fig4: ICC staining of ATF2 in MCF-7 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1603-15, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |
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Fig5: ICC staining of ATF2 in PC-12 cells (green). Formalin fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 10 minutes at room temperature and blocked with 10% negative goat serum for 15 minutes at room temperature. Cells were probed with the primary antibody (ET1603-15, 1/50) for 1 hour at room temperature, washed with PBS. Alexa Fluor®488 conjugate-Goat anti-Rabbit IgG was used as the secondary antibody at 1/1,000 dilution. The nuclear counter stain is DAPI (blue). |
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Fig6:
Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue with Rabbit anti-ATF2 antibody (ET1603-15) at 1/200 dilution. The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (ET1603-15) at 1/200 dilution for 1 hour 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. |