Human/Mouse Phospho-STAT1 (Y701) Antibody
R&D Systems | Catalog # AF2894
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Scientific Data Images for Human/Mouse Phospho-STAT1 (Y701) Antibody
Detection of Human Phospho-STAT1 (Y701) by Western Blot.
Western blot shows lysates of Daudi human Burkitt's lymphoma cell line untreated (-) or treated (+) with Recombinant Human IFN-a2a for 20 minutes. PVDF membrane was probed with 0.5 µg/mL of Rabbit Anti-Human/Mouse Phospho-STAT1 (Y701) Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2894), followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog # HAF008). A specific band was detected for Phospho-STAT1 (Y701) at approximately 94 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 2.
Detection of Phospho-STAT1 in IFN-alpha -treated Daudi Human Cell Line by Flow Cytometry.
Daudi human Burkitt's lymphoma cell line was unstimulated (light orange filled histogram) or treated with 500 units/mL Recombinant Human IFN-a (Catalog # 11100-1) for 20 minutes (dark orange filled histogram), then stained with Rabbit Anti-Human/Mouse Phospho-STAT1 (Y701) Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2894) or control antibody (Catalog # AB-105-C, open histogram), followed by Allophycocyanin-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog # F0111). To facilitate intracellular staining, cells were fixed with paraformaldehyde and permeabilized with methanol.
Detection of Human Phospho-STAT1 (Y701) by Simple WesternTM.
Simple Western lane view shows lysates of Daudi human Burkitt's lymphoma cell line untreated (-) or treated (+) with Recombinant Human IFN-aA (Catalog # 11100-1) for 20 minutes, loaded at 0.2 mg/mL. A specific band was detected for Phospho-STAT1 (Y701) at approximately 86 kDa (as indicated) using 5 µg/mL of Rabbit Anti-Human/Mouse Phospho-STAT1 (Y701) Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2894). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.
Detection of Mouse STAT1 by Western Blot
Effects of kurarinone on the phosphorylation of p-STAT1 and p-STAT3 in lymph nodes. Single cell suspensions were collected from ILNs on day 42, the protein expression levels of p-STAT1, STAT1, p-STAT3, and STAT3 were measured using Western blots. (A) Representative images of Western blot and (B) Densitometric analysis for protein expressions was performed using ImageJ software. Data are presented as mean ± SEM of 6 mice from one of three experiments. (*) p < 0.05, (**) p < 0.01, (***) p < 0.001 versus vehicle-treated CIA mice group (One Way ANOVA followed by Tukey’s multiple comparison test). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/33924467), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Phospho-STAT1 (Y701) by Western Blot
The loss of C9ORF72 leads to JAK-STAT activation(A) RT-qPCR analysis of Sting levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗p < 0.05, ∗∗p < 0.01.(B) Protein levels of STAT1 in spleen lysates from 6-month-old WT and C9orf72−/− mice were analyzed using western blot. Mixed male and female mice were used. Data represent the mean ± SEM. Statistical significance was analyzed by unpaired one-tail Student’s t test (n = 4), ns = not significant, ∗p < 0.05.(C) Protein levels of STAT1 and p-STAT1 in control or C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 2h were analyzed using western blot and normalized to GAPDH. Data represent the mean ± SEM. Statistical significance was analyzed by unpaired two-tail Student’s t test (n = 3), ns = not significant, ∗p < 0.05.(D) RT-qPCR analysis of Stat1 levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗p < 0.05, ∗∗∗∗p < 0.0001.(E) IFN-beta levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h were measured using ELISA. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗∗p < 0.01. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37250330), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Phospho-STAT1 (Y701) by Western Blot
The loss of C9ORF72 leads to JAK-STAT activation(A) RT-qPCR analysis of Sting levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗p < 0.05, ∗∗p < 0.01.(B) Protein levels of STAT1 in spleen lysates from 6-month-old WT and C9orf72−/− mice were analyzed using western blot. Mixed male and female mice were used. Data represent the mean ± SEM. Statistical significance was analyzed by unpaired one-tail Student’s t test (n = 4), ns = not significant, ∗p < 0.05.(C) Protein levels of STAT1 and p-STAT1 in control or C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 2h were analyzed using western blot and normalized to GAPDH. Data represent the mean ± SEM. Statistical significance was analyzed by unpaired two-tail Student’s t test (n = 3), ns = not significant, ∗p < 0.05.(D) RT-qPCR analysis of Stat1 levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗p < 0.05, ∗∗∗∗p < 0.0001.(E) IFN-beta levels in control and C9orf72−/− RAW264.7 cells untreated or treated with DMXAA for 16h were measured using ELISA. Data represent the mean ± SEM. Statistical significance was analyzed by two-way ANOVA (n = 3), ns = not significant, ∗∗p < 0.01. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37250330), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human/Mouse Phospho-STAT1 (Y701) Antibody
CyTOF-ready
Intracellular Staining by Flow Cytometry
Sample: IFN-alpha -treated Daudi human Burkitt's lymphoma cell line fixed with paraformaldehyde and permeabilized with methanol
Simple Western
Sample: Daudi human Burkitt's lymphoma cell line treated with Recombinant Human IFN‑ alpha A (Catalog # 11100-1)
Western Blot
Sample: Daudi human Burkitt's lymphoma cell line treated with Recombinant Human IFN-alpha 2a
Reviewed Applications
Read 9 reviews rated 4.4 using AF2894 in the following applications:
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
Purification
Reconstitution
Reconstitute at 0.2 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: STAT1
Long Name
Alternate Names
Gene Symbol
Additional STAT1 Products
Product Documents for Human/Mouse Phospho-STAT1 (Y701) Antibody
Product Specific Notices for Human/Mouse Phospho-STAT1 (Y701) Antibody
For research use only
Citations for Human/Mouse Phospho-STAT1 (Y701) Antibody
Customer Reviews for Human/Mouse Phospho-STAT1 (Y701) Antibody (9)
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Customer Images
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Application: Western BlotSample Tested: THP-1 human acute monocytic leukemia cell lineSpecies: HumanVerified Customer | Posted 10/12/2025
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Application: Western BlotSample Tested: RAW 264.7 mouse monocyte/macrophage cell lineSpecies: MouseVerified Customer | Posted 03/28/2023First antibody: 1:2000, 4 oC, overnight Second antibody: 1:5000, room temperature, 1 h
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Application: Western BlotSample Tested: MDA-MB-231 human breast cancer cell lineSpecies: HumanVerified Customer | Posted 04/18/2022
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Application: Western BlotSample Tested: Human lung macrophages and JurkatSpecies: HumanVerified Customer | Posted 04/04/2020
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Application: MicroarraysSample Tested: EDTA PlasmaSpecies: HumanVerified Customer | Posted 03/11/2019
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Application: ImmunohistochemistrySample Tested: Breast cancer tissueSpecies: HumanVerified Customer | Posted 02/19/2019
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Application: ELISASample Tested: Serum and PlasmaSpecies: Human and MouseVerified Customer | Posted 11/08/2018
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Application: MicroarraySample Tested: EDTA PlasmaSpecies: HumanVerified Customer | Posted 11/02/2018
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Application: Western BlotSample Tested: EMT6 cells and CT26Species: MouseVerified Customer | Posted 10/17/2018
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
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