Anti-Progesterone Receptor抗体[Alpha PR6]
参阅全部 Progesterone Receptor 一抗
小鼠单克隆抗体[Alpha PR6] to Progesterone Receptor
Mouse
Detects the B form of the progesterone receptor (PR). This antibody does not cross-react with estrogen receptor or glucocorticoid receptor.
适用于: IHC-P, WB, Flow Cyt, ICC/IFmore details
与反应: Human
Full length protein corresponding to Chicken Progesterone Receptor. Progesterone receptor purified from chick oviduct cytosol.
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Liquid
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
Preservative: 0.05% Sodium azide
Constituent: PBS
Protein G purified
单克隆
Alpha PR6
IgG2a
Abpromise™承诺保证使用ab2765于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
IHC-P | (5) | Use a concentration of 5 µg/ml. |
WB | Use a concentration of 1 µg/ml. Predicted molecular weight: 99 kDa. | |
Flow Cyt | Use 0.5µg for 106 cells. ab170191 - Mouse monoclonal IgG2a, is suitable for use as an isotype control with this antibody. | |
ICC/IF | (1) | Use at an assay dependent concentration. |
Entrez Gene: 5241 Human
Omim: 607311 Human
SwissProt: P06401 Human
Unigene: 32405 Human
Unigene: 742403 Human
PR antibody
PRA antibody
PRB antibody
PRGR_HUMAN antibody
Progesterone receptor antibody
Progestin receptor form A antibody
Progestin receptor form B antibody
NR3C3 antibody
Nuclear receptor subfamily 3 group C member 3 antibody
PGR antibody
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Progesterone Receptor antibody [Alpha PR6] (ab2765)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) was performed on human uterus tissue. Antigen retrieval was performed using 10mM sodium citrate followed by microwave treatment for 8-15 minutes. Endogenous peroxidases were blocked in 3% H202-methanol for 15 minutes and tissues were blocked in 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with ab2765 (1:20) overnight in a humidified chamber. Tissues were washed in PBST and detection was performed using a secondary antibody conjugated to HRP. DAB staining buffer was applied and tissues were counterstained with hematoxylin and prepped for mounting. Images were taken at 40X magnification.
Immunocytochemistry/ Immunofluorescence - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)
Immunocytochemistry/ Immunofluorescence analysis of T47D cells untreated (left) or stimulated with 100nm promegestone for 1 hour (right), labeling Progesterone Receptor with ab2765 (green). The cells were fixed with formalin for 15 minutes, permeabilized with 0.1% Triton X-100 in TBS for 10 minutes, and blocked with 3% Blocker BSA for 15 minutes at room temperature. Cells were stained with Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765) at a dilution of 1/100 for 1 hour at 37C, and then incubated with a Alexa Fluor 488 goat anti-mouse IgG secondary antibody at a dilution of 1/1000 for 30 minutes at room temperature (both panels, green). Nuclei (both panels, blue) were stained with Hoechst 33342 dye.
Western blot - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)
All lanes : Anti-Progesterone Receptor antibody [Alpha PR6] (ab2765) at 1 µg/ml
Lane 1 : T47D cell lysate untreated (-)
Lane 2 : T47D cell lysate stimulated (+) with 100 nm promegestone for 1 hour
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat anti-Mouse IgG-HRP at 1/2000 dilution
Predicted band size: 99 kDa
Flow Cytometry - Anti-Progesterone Receptor antibody [Alpha PR6] - ChIP Grade (ab2765)
Overlay histogram showing T47D cells stained with ab2765 (red line). The cells were fixed with 80% methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab2765, 0.5µg/1x106 cells) for 30 min at 22ºC. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22ºC. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed.