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heag1 polyclonal antibody  (Alomone Labs)


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    Alomone Labs heag1 polyclonal antibody
    Figure 2. Determination of the titer of <t>hEAG1</t> polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.
    Heag1 Polyclonal Antibody, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 9 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/heag1+polyclonal+antibody/Anti-KCNH1+(EAG-1)+Antibody/pm22248279-74-12-22
    Average 93 stars, based on 9 article reviews
    heag1 polyclonal antibody - by Bioz Stars, 2026-09
    93/100 stars

    Images

    1) Product Images from "Overexpression of potassium channel ether à go-go in human osteosarcoma."

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    Journal: Neoplasma

    doi: 10.4149/neo_2012_027

    Figure 2. Determination of the titer of hEAG1 polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.
    Figure Legend Snippet: Figure 2. Determination of the titer of hEAG1 polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.

    Techniques Used: Enzyme-linked Immunosorbent Assay, Positive Control, Negative Control

    Figure 4. Analysis of the immunoreactivity of hEAG1 antibodies by Western blot. Mouse brain extracts were prepared, separated on SDS-PAGE and trans- ferred on PVDF membrane as described in Materials. Membranes were immunolabelled with the polyclonal antibody we generated (diluted 1:1000, lane 1), or with the commercial hEAG1 antibody (diluted 1:200, lane 2). The bands revealed by both antibodies had a molecular weight between 150 and 100 kDa. M: marker.
    Figure Legend Snippet: Figure 4. Analysis of the immunoreactivity of hEAG1 antibodies by Western blot. Mouse brain extracts were prepared, separated on SDS-PAGE and trans- ferred on PVDF membrane as described in Materials. Membranes were immunolabelled with the polyclonal antibody we generated (diluted 1:1000, lane 1), or with the commercial hEAG1 antibody (diluted 1:200, lane 2). The bands revealed by both antibodies had a molecular weight between 150 and 100 kDa. M: marker.

    Techniques Used: Western Blot, SDS Page, Membrane, Generated, Molecular Weight, Marker

    Figure 3. Analysis of the activity and specificity of hEAG1 polyclonal antibody by Western blot. (A) Western blot showing the activity of hEAG1 polyclonal anti- body. Lane 1, lysate of E. coli BL21(DE3) cells harboring pRSET-A- hEAG1F after induction; Lane 2, lysate of HEK 293 cells transfected by pcDNA3.1-hEAG1; Lane 3, lysate of HEK 293 cells transfected by pcDNA3.1(+) empty vector. (B) Western blot showing the specificity of hEAG1 polyclonal antibody. Lysate of HEK293 cells transfected by pcDNA3.1 empty vector, pcDNA3.1-hEAG1 or pcDNA3.1-hEAG2 was detected by the indicated antibodies.
    Figure Legend Snippet: Figure 3. Analysis of the activity and specificity of hEAG1 polyclonal antibody by Western blot. (A) Western blot showing the activity of hEAG1 polyclonal anti- body. Lane 1, lysate of E. coli BL21(DE3) cells harboring pRSET-A- hEAG1F after induction; Lane 2, lysate of HEK 293 cells transfected by pcDNA3.1-hEAG1; Lane 3, lysate of HEK 293 cells transfected by pcDNA3.1(+) empty vector. (B) Western blot showing the specificity of hEAG1 polyclonal antibody. Lysate of HEK293 cells transfected by pcDNA3.1 empty vector, pcDNA3.1-hEAG1 or pcDNA3.1-hEAG2 was detected by the indicated antibodies.

    Techniques Used: Activity Assay, Western Blot, Transfection, Plasmid Preparation

    Figure 5. Immunofluorescence analysis of hEAG1 subcellular localization by hEAG1 polyclonal antibody. HEK293 cells were either mock transfected with pcDNA3.1(+) or transfected with pcDNA3-hEAG1, and then stained with hEAG1 polyclonal antibody. Positive hEAG1 staining was red and DAPI (indicating the nucleus) was blue. The scale bar: 10 μm.
    Figure Legend Snippet: Figure 5. Immunofluorescence analysis of hEAG1 subcellular localization by hEAG1 polyclonal antibody. HEK293 cells were either mock transfected with pcDNA3.1(+) or transfected with pcDNA3-hEAG1, and then stained with hEAG1 polyclonal antibody. Positive hEAG1 staining was red and DAPI (indicating the nucleus) was blue. The scale bar: 10 μm.

    Techniques Used: Transfection, Staining

    Figure 6. Immunohistochemical staining of hEAG1 in human osteosar- coma samples. hEAG1 immunostaining was detected in a human brain specimen (positive control, A) , 71.4% of human osteosarcoma specimens (B) and (15.8%) osteochondromas specimens (C). Images were captured using an OL- YMPUS light microscope equipped with a CCD colour camera at a 400× magnification. The scale bar: 50 μm.
    Figure Legend Snippet: Figure 6. Immunohistochemical staining of hEAG1 in human osteosar- coma samples. hEAG1 immunostaining was detected in a human brain specimen (positive control, A) , 71.4% of human osteosarcoma specimens (B) and (15.8%) osteochondromas specimens (C). Images were captured using an OL- YMPUS light microscope equipped with a CCD colour camera at a 400× magnification. The scale bar: 50 μm.

    Techniques Used: Immunohistochemical staining, Staining, Immunostaining, Positive Control, Light Microscopy

    Related Articles

    Western Blot:

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.
    Article Snippet: The membranes were incubated overnight at 4°C with either hEAG1 polyclonal antibody we generated (1:1000) or hEAG2 antibody (SAB2104244, Sigma, USA) in blocking solution, then with horseradish peroxidase (HRP) conjugated goat anti-mouse antibody (1:10,000) or goat anti-rabbit antibody (1:15,000), and finally developed by enhanced chemiluminescence system. .. Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein. ..

    Generated:

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.
    Article Snippet: The membranes were incubated overnight at 4°C with either hEAG1 polyclonal antibody we generated (1:1000) or hEAG2 antibody (SAB2104244, Sigma, USA) in blocking solution, then with horseradish peroxidase (HRP) conjugated goat anti-mouse antibody (1:10,000) or goat anti-rabbit antibody (1:15,000), and finally developed by enhanced chemiluminescence system. .. Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein. ..

    Expressing:

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.
    Article Snippet: The membranes were incubated overnight at 4°C with either hEAG1 polyclonal antibody we generated (1:1000) or hEAG2 antibody (SAB2104244, Sigma, USA) in blocking solution, then with horseradish peroxidase (HRP) conjugated goat anti-mouse antibody (1:10,000) or goat anti-rabbit antibody (1:15,000), and finally developed by enhanced chemiluminescence system. .. Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein. ..



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    Alomone Labs heag1 polyclonal antibody
    Figure 2. Determination of the titer of <t>hEAG1</t> polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.
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    Figure 2. Determination of the titer of <t>hEAG1</t> polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.
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    Image Search Results


    Figure 2. Determination of the titer of hEAG1 polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.

    Journal: Neoplasma

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    doi: 10.4149/neo_2012_027

    Figure Lengend Snippet: Figure 2. Determination of the titer of hEAG1 polyclonal antibody by ELISA. (A) The antibody was diluted serially as shown on the top. Positive control was anti-His antibody; Negative control was pre-immunized rabbit serum. (B) Quantization of absorbance values shown in Fig. 2A.

    Article Snippet: Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein.

    Techniques: Enzyme-linked Immunosorbent Assay, Positive Control, Negative Control

    Figure 4. Analysis of the immunoreactivity of hEAG1 antibodies by Western blot. Mouse brain extracts were prepared, separated on SDS-PAGE and trans- ferred on PVDF membrane as described in Materials. Membranes were immunolabelled with the polyclonal antibody we generated (diluted 1:1000, lane 1), or with the commercial hEAG1 antibody (diluted 1:200, lane 2). The bands revealed by both antibodies had a molecular weight between 150 and 100 kDa. M: marker.

    Journal: Neoplasma

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    doi: 10.4149/neo_2012_027

    Figure Lengend Snippet: Figure 4. Analysis of the immunoreactivity of hEAG1 antibodies by Western blot. Mouse brain extracts were prepared, separated on SDS-PAGE and trans- ferred on PVDF membrane as described in Materials. Membranes were immunolabelled with the polyclonal antibody we generated (diluted 1:1000, lane 1), or with the commercial hEAG1 antibody (diluted 1:200, lane 2). The bands revealed by both antibodies had a molecular weight between 150 and 100 kDa. M: marker.

    Article Snippet: Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein.

    Techniques: Western Blot, SDS Page, Membrane, Generated, Molecular Weight, Marker

    Figure 3. Analysis of the activity and specificity of hEAG1 polyclonal antibody by Western blot. (A) Western blot showing the activity of hEAG1 polyclonal anti- body. Lane 1, lysate of E. coli BL21(DE3) cells harboring pRSET-A- hEAG1F after induction; Lane 2, lysate of HEK 293 cells transfected by pcDNA3.1-hEAG1; Lane 3, lysate of HEK 293 cells transfected by pcDNA3.1(+) empty vector. (B) Western blot showing the specificity of hEAG1 polyclonal antibody. Lysate of HEK293 cells transfected by pcDNA3.1 empty vector, pcDNA3.1-hEAG1 or pcDNA3.1-hEAG2 was detected by the indicated antibodies.

    Journal: Neoplasma

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    doi: 10.4149/neo_2012_027

    Figure Lengend Snippet: Figure 3. Analysis of the activity and specificity of hEAG1 polyclonal antibody by Western blot. (A) Western blot showing the activity of hEAG1 polyclonal anti- body. Lane 1, lysate of E. coli BL21(DE3) cells harboring pRSET-A- hEAG1F after induction; Lane 2, lysate of HEK 293 cells transfected by pcDNA3.1-hEAG1; Lane 3, lysate of HEK 293 cells transfected by pcDNA3.1(+) empty vector. (B) Western blot showing the specificity of hEAG1 polyclonal antibody. Lysate of HEK293 cells transfected by pcDNA3.1 empty vector, pcDNA3.1-hEAG1 or pcDNA3.1-hEAG2 was detected by the indicated antibodies.

    Article Snippet: Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein.

    Techniques: Activity Assay, Western Blot, Transfection, Plasmid Preparation

    Figure 5. Immunofluorescence analysis of hEAG1 subcellular localization by hEAG1 polyclonal antibody. HEK293 cells were either mock transfected with pcDNA3.1(+) or transfected with pcDNA3-hEAG1, and then stained with hEAG1 polyclonal antibody. Positive hEAG1 staining was red and DAPI (indicating the nucleus) was blue. The scale bar: 10 μm.

    Journal: Neoplasma

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    doi: 10.4149/neo_2012_027

    Figure Lengend Snippet: Figure 5. Immunofluorescence analysis of hEAG1 subcellular localization by hEAG1 polyclonal antibody. HEK293 cells were either mock transfected with pcDNA3.1(+) or transfected with pcDNA3-hEAG1, and then stained with hEAG1 polyclonal antibody. Positive hEAG1 staining was red and DAPI (indicating the nucleus) was blue. The scale bar: 10 μm.

    Article Snippet: Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein.

    Techniques: Transfection, Staining

    Figure 6. Immunohistochemical staining of hEAG1 in human osteosar- coma samples. hEAG1 immunostaining was detected in a human brain specimen (positive control, A) , 71.4% of human osteosarcoma specimens (B) and (15.8%) osteochondromas specimens (C). Images were captured using an OL- YMPUS light microscope equipped with a CCD colour camera at a 400× magnification. The scale bar: 50 μm.

    Journal: Neoplasma

    Article Title: Overexpression of potassium channel ether à go-go in human osteosarcoma.

    doi: 10.4149/neo_2012_027

    Figure Lengend Snippet: Figure 6. Immunohistochemical staining of hEAG1 in human osteosar- coma samples. hEAG1 immunostaining was detected in a human brain specimen (positive control, A) , 71.4% of human osteosarcoma specimens (B) and (15.8%) osteochondromas specimens (C). Images were captured using an OL- YMPUS light microscope equipped with a CCD colour camera at a 400× magnification. The scale bar: 50 μm.

    Article Snippet: Moreover, Western blot analysis was also used to test the immunoreacitivity of hEAG1 polyclonal antibody we generated and commercial hEAG1 antibody (APC-104, Alomone Labs, Israel, 1:200) performed on protein extracts obtained from mouse brain, a tissue highly expressing hEAG1 protein.

    Techniques: Immunohistochemical staining, Staining, Immunostaining, Positive Control, Light Microscopy