Product Type: | Recombinant Mouse monoclonal IgG1, primary antibodies |
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Species reactivity: | Human |
Applications: | WB, IHC-P |
Clonality: | Monoclonal |
Clone number: | G3-B11-R |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Protein A affinity purified. |
Molecular weight: | Predicted band size: 87/83 kDa |
Isotype: | IgG1 |
Immunogen: | Recombinant protein within Human STAT1 aa 71-270 / 750. |
Positive control: | Jurkat cell lysate, A431 cell lysate, HeLa cell lysate, A549 cell lysate, SK-Br-3 cell lysate, SK-MEL-28 cell lysate, MCF7 cell lysate, HT-29 cell lysate, human breast cancer tissue, human spleen tissue. |
Subcellular location: | Cytoplasm, nucleus |
Recommended Dilutions:
WB IHC-P |
1:1,000 1:1,000 |
Uniprot #: | SwissProt: P42224 Human |
Alternative names: | Signal transducer and activator of transcription 1 91kD CANDF7 DKFZp686B04100 IMD31A IMD31B IMD31C ISGF 3 ISGF-3 OTTHUMP00000163552 OTTHUMP00000165046 OTTHUMP00000165047 OTTHUMP00000205845 Signal transducer and activator of transcription 1 91kDa Signal transducer and activator of transcription 1 Signal transducer and activator of transcription 1, 91kD Signal transducer and activator of transcription 1-alpha/beta STAT 1 Stat1 STAT1_HUMAN STAT91 Transcription factor ISGF 3 components p91 p84 Transcription factor ISGF-3 components p91/p84 |
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Fig1:
Western blot analysis of STAT1 on different lysates with Mouse anti-STAT1 antibody (HA601309) at 1/1,000 dilution. Lane 1: Jurkat cell lysate Lane 2: A431 cell lysate Lane 3: HeLa cell lysate Lane 4: A549 cell lysate Lane 5: SK-Br-3 cell lysate Lane 6: SK-MEL-28 cell lysate Lane 7: MCF7 cell lysate Lane 8: HT-29 cell lysate Lysates/proteins at 15 µg/Lane. Predicted band size: 87/83 kDa Observed band size: 87/83 kDa Exposure time: 30 seconds; ECL: K1802; 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 (HA601309) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Mouse IgG - HRP Secondary Antibody (HA1006) at 1/50,000 dilution was used for 1 hour at room temperature. |
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Fig2:
Western blot analysis of STAT1 on different lysates with Mouse anti-APE1 antibody (HA601309) at 1/1,000 dilution. Lane 1: PATU8988-parental cell lysate Lane 2: PATU8988-STAT1 KD cell lysate Lysates/proteins at 10 µg/Lane. Predicted band size: 87/83 kDa Observed band size: 83 kDa Exposure time: 15 seconds; 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 (HA601309)) at 1/1,000 dilution was used in primary antibody dilution (K1803) 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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Fig3:
Immunohistochemical analysis of paraffin-embedded human breast cancer tissue with Mouse anti-STAT1 antibody (HA601309) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (HA601309) at 1/1,000 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. |
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Fig4:
Immunohistochemical analysis of paraffin-embedded human spleen tissue with Mouse anti-STAT1 antibody (HA601309) at 1/1,000 dilution. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) for 2 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 (HA601309) at 1/1,000 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. |