Product Type: | Recombinant Rabbit monoclonal IgG, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IF-Cell, IF-Tissue, IHC-P, FC |
Clonality: | Monoclonal |
Clone number: | JJ207-04 |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃ or -80℃. Avoid repeated freeze / thaw cycles. |
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: 29 kDa |
Isotype: | IgG |
Immunogen: | Synthetic peptide within Human ATF1 aa 222-271 / 271. |
Positive control: | HUVEC, Hela, human lung cancer tissue, human breast carcinoma tissue. |
Subcellular location: | Nucleus. |
Recommended Dilutions:
WB IF-Cell IF-Tissue IHC-P FC |
1;500-1:1,000 1:50-1:200 1:50-1:200 1:50-1:200 1:50-1:100 |
Uniprot #: | SwissProt: P18846 Human |
Alternative names: | Activating transcription factor 1 ATF 1 atf1 ATF1 EWS fusion gene ATF1 FUS fusion gene ATF1_HUMAN cAMP dependent transcription factor 1 cAMP-dependent transcription factor ATF-1 Cyclic AMP dependent transcription factor ATF 1 Cyclic AMP dependent transcription factor ATF1 Cyclic AMP-dependent transcription factor ATF-1 EWS AFT1 FUS ATF 1 FUS/ATF 1 Protein TREB36 RNA binding protein activating transcription factor 1 fusion protein TREB 36 TREB36 TREB36 protein |
Fig1:
Western blot analysis of ATF1 on different lysates with Rabbit anti-ATF1 antibody (ET1701-30) at 1/2,000 dilution. Lane 1: A549-WT cell lysate Lane 2: A549-KD ATF1 cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 29 kDa Observed band size: 35 kDa Exposure time: 2 minutes; 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 (ET1701-30) at 1/2,000 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 ATF1 in HUVEC cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. | |
Fig3: ICC staining ATF1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS. |
Fig4: Immunohistochemical analysis of paraffin-embedded human lung cancer tissue using anti-ATF1 antibody. Counter stained with hematoxylin. | |
Fig5: Immunohistochemical analysis of paraffin-embedded human breast carcinoma tissue using anti-ATF1 antibody. Counter stained with hematoxylin. | |
Fig6: Flow cytometric analysis of Hela cells with ATF1 antibody at 1/50 dilution (red) compared with an unlabelled control (cells without incubation with primary antibody; black). Alexa Fluor 488-conjugated goat anti rabbit IgG was used as the secondary antibody. |