Anti-Endothelin 1抗体[TR.ET.48.5]
参阅全部 Endothelin 1 一抗
小鼠单克隆抗体[TR.ET.48.5] to Endothelin 1
Mouse
Immunohistochemical staining of ET-1 in human corpus cavernosum tissue with this antibody results in staining of endothelial cells. Radioimmune assays can be used to concentrate ET-1 in solution (e.g. serum/plasma, milk, urine).
适用于: Flow Cyt, ICC/IF, IHC-P, WBmore details
与反应: Mouse, Rat, Human
Full length native protein (purified) corresponding to Human Endothelin 1 conjugated to keyhole limpet haemocyanin.
Studies suggest that this antibody binds to an epitope in the region of ET-1 represented by amino acids 8-16.
human bowel
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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
浓度
100 µl 浓度为 2.5 mg/ml
Protein G purified
单克隆
TR.ET.48.5
IgG1
Abpromise™承诺保证使用ab2786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 |
---|---|---|
Flow Cyt | Use at an assay dependent concentration. ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. | |
ICC/IF | 1/200 - 1/1000. | |
IHC-P | 1/250. | |
WB | Use at an assay dependent concentration. Predicted molecular weight: 24 kDa. |
Entrez Gene: 1906 Human
Entrez Gene: 13614 Mouse
Omim: 131240 Human
SwissProt: P05305 Human
SwissProt: P22387 Mouse
Unigene: 511899 Human
Unigene: 713645 Human
ARCND3 antibody
Big endothelin-1 antibody
EDN1 antibody
EDN1_HUMAN antibody
ET-1 antibody
ET1 antibody
HDLCQ7 antibody
PPET1 antibody
Preproendothelin 1 antibody
Preproendothelin-1 antibody
QME antibody
Immunocytochemistry/ Immunofluorescence - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
ab2786 labelling Endothelin 1 (green) in the secretion of HeLa cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Blue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Western blot - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786) at 1/500 dilution + PC12 cell lysate at 25 µg
Predicted band size: 24 kDa
Observed band size: 30 kDawhy is the actual band size different from the predicted?
Flow Cytometry - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
Flow cytometry analysis of Endothelin 1 showing positive staining in the cytoplasm of 293T cells compared to an isotype control (blue). Cells were harvested, adjusted to a concentration of 1-5x10^6 cells/ml, fixed with 2% paraformaldehyde, washed with PBS, and incubated with ab2786 (0.5 ug/test) for 60 min at room temperature. Cells were then blocked in a solution of 2% BSA-PBS for 30 min at room temperature, incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody, and re-suspended in PBS for FACS analysis.
Immunocytochemistry/ Immunofluorescence - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
ab2786 labelling Endothelin 1 (green) in the secretion of PC12 cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Blue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Flow Cytometry - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
Flow cytometry analysis of Endothelin 1 showing positive staining in the cytoplasm of HepG2 cells compared to an isotype control (blue). Cells were harvested, adjusted to a concentration of 1-5x10^6 cells/ml, fixed with 2% paraformaldehyde, washed with PBS, and incubated with ab2786 (0.5 ug/test) for 60 min at room temperature. Cells were then blocked in a solution of 2% BSA-PBS for 30 min at room temperature, incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody, and re-suspended in PBS for FACS analysis.
Immunocytochemistry/ Immunofluorescence - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
ab2786 labelling Endothelin 1 (green) in the secretion of HUVEC cells (right) compared with a negative control (left) by Immunocytochemistry/Immunofluorescence. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were incubated with the primary antibody (1:200 in 3% BSA-PBS) overnight at 4 ºC. A DyLight 488-conjugated Goat anti-mouse IgG (H+L) was used as the secondary antibody. Red (phalloidin) - F-actin, Blue (DAPI) - nuclei. Images were taken at a magnification of 60x.
Flow Cytometry - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
Flow cytometry analysis of Endothelin 1 showing positive staining in the cytoplasm of 3T3 cells compared to an isotype control (blue). Cells were harvested, adjusted to a concentration of 1-5x10^6 cells/ml, fixed with 2% paraformaldehyde, washed with PBS, and incubated with ab2786 (0.5 ug/test) for 60 min at room temperature. Cells were then blocked in a solution of 2% BSA-PBS for 30 min at room temperature, incubated for 40 min at room temperature in the dark using a Dylight 488-conjugated goat anti-mouse IgG (H+L) secondary antibody, and re-suspended in PBS for FACS analysis.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Endothelin 1 antibody [TR.ET.48.5] (ab2786)
Figure 1 and Figure 2 show immunolocalization of ET-1 in human bowel using ab2786.
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