anti adra1b  (Alomone Labs)


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    Name:
    Anti alpha1B Adrenergic Receptor extracellular Antibody
    Description:
    Anti α1B Adrenergic Receptor extracellular Antibody AAR 018 is a highly specific antibody directed against an extracellular epitope of the human α1B adrenoceptor The antibody can be used in western blot immunohistochemistry live cell imaging and indirect flow cytometry applications It has been designed to recognize α1B adrenoceptor from human rat and mouse samples
    Catalog Number:
    AAR-018
    Price:
    495.0
    Category:
    Primary Antibody
    Applications:
    Immunocytochemistry, Immunofluorescence, Indirect Flow Cytometry, Immunohistochemistry, Live Cell Imaging, Western Blot
    Purity:
    Affinity purified on immobilized antigen.
    Immunogen:
    Synthetic peptide
    Size:
    50 mcl
    Antibody Type:
    Polyclonal Primary Antibodies
    Format:
    Lyophilized Powder
    Host:
    Rabbit
    Isotype:
    Rabbit IgG
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    Structured Review

    Alomone Labs anti adra1b
    Anti alpha1B Adrenergic Receptor extracellular Antibody
    Anti α1B Adrenergic Receptor extracellular Antibody AAR 018 is a highly specific antibody directed against an extracellular epitope of the human α1B adrenoceptor The antibody can be used in western blot immunohistochemistry live cell imaging and indirect flow cytometry applications It has been designed to recognize α1B adrenoceptor from human rat and mouse samples
    https://www.bioz.com/result/anti adra1b/product/Alomone Labs
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti adra1b - by Bioz Stars, 2021-10
    90/100 stars

    Images

    1) Product Images from "L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor"

    Article Title: L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor

    Journal: JCI Insight

    doi: 10.1172/jci.insight.90903

    Interaction between GPR143 and ADRA1B. ( A ) Co-immunoprecipitation (Co-IP) of ADRA1B-Myc and GPR143-HA. Bands were detected by anti-Myc (left) or by anti-HA (right) antibodies. ( B ) Protein levels of pERK and whole ERK 10 minutes after the treatment with phenylephrine. ( C ) Summarized data of pERK/ERK (% of control) in HEK293 cells coexpressing ADRA1B-Myc and free-EGFP or ADRA1B-Myc and GPR143-EGFP ( F 1,32 = 7.899, P
    Figure Legend Snippet: Interaction between GPR143 and ADRA1B. ( A ) Co-immunoprecipitation (Co-IP) of ADRA1B-Myc and GPR143-HA. Bands were detected by anti-Myc (left) or by anti-HA (right) antibodies. ( B ) Protein levels of pERK and whole ERK 10 minutes after the treatment with phenylephrine. ( C ) Summarized data of pERK/ERK (% of control) in HEK293 cells coexpressing ADRA1B-Myc and free-EGFP or ADRA1B-Myc and GPR143-EGFP ( F 1,32 = 7.899, P

    Techniques Used: Immunoprecipitation, Co-Immunoprecipitation Assay

    Immunohistochemical staining of endogenous GPR143 and ADRA1B. Expression of GPR143 ( A ) and ADRA1B ( C ) in the liver (arrowheads). No GPR143 signals were observed in the liver of Gpr143 –/y mice ( B ). No ADRA1B signals were observed in sections incubated with the antigenic peptide–preadsorbed antibody ( D ). Scale bar: 100 μm. Endogenous interaction between GPR143 and ADRA1B. ( E ) The GPR143-ADRA1B interacting signals (green) were detected by in situ proximity ligation assay technology in WT liver (arrowheads). ( F ) No interacting signals were observed in Gpr143 –/y liver ( n = 2, independent experiments). The nucleus was counterstained by DAPI (blue). Scale bars: 5 μm.
    Figure Legend Snippet: Immunohistochemical staining of endogenous GPR143 and ADRA1B. Expression of GPR143 ( A ) and ADRA1B ( C ) in the liver (arrowheads). No GPR143 signals were observed in the liver of Gpr143 –/y mice ( B ). No ADRA1B signals were observed in sections incubated with the antigenic peptide–preadsorbed antibody ( D ). Scale bar: 100 μm. Endogenous interaction between GPR143 and ADRA1B. ( E ) The GPR143-ADRA1B interacting signals (green) were detected by in situ proximity ligation assay technology in WT liver (arrowheads). ( F ) No interacting signals were observed in Gpr143 –/y liver ( n = 2, independent experiments). The nucleus was counterstained by DAPI (blue). Scale bars: 5 μm.

    Techniques Used: Immunohistochemistry, Staining, Expressing, Mouse Assay, Incubation, In Situ, Proximity Ligation Assay

    Related Articles

    Incubation:

    Article Title: Cisplatin alters the function and expression of N-type voltage-gated calcium channels in the absence of morphological damage of sensory neurons
    Article Snippet: .. Membranes were incubated overnight at 4℃ with rabbit polyclonal N-type alpha 1B (1:200, Alomone Labs) and mouse monoclonal beta-actin (1:1000, Thermo Fisher Scientific) antibodies. ..

    Article Title: L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor
    Article Snippet: .. The sections were incubated with anti-TH (#22941, ImmunoStar) antibody, anti-GPR143 antibody , or anti-ADRA1B (#AAR-018, Alomone Labs) antibody at 4°C for 24 hours. ..

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  • 90
    Alomone Labs anti adra1b
    Interaction between GPR143 and <t>ADRA1B.</t> ( A ) Co-immunoprecipitation (Co-IP) of ADRA1B-Myc and GPR143-HA. Bands were detected by anti-Myc (left) or by anti-HA (right) antibodies. ( B ) Protein levels of pERK and whole ERK 10 minutes after the treatment with phenylephrine. ( C ) Summarized data of pERK/ERK (% of control) in HEK293 cells coexpressing ADRA1B-Myc and free-EGFP or ADRA1B-Myc and GPR143-EGFP ( F 1,32 = 7.899, P
    Anti Adra1b, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti adra1b/product/Alomone Labs
    Average 90 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti adra1b - by Bioz Stars, 2021-10
    90/100 stars
      Buy from Supplier

    Image Search Results


    Interaction between GPR143 and ADRA1B. ( A ) Co-immunoprecipitation (Co-IP) of ADRA1B-Myc and GPR143-HA. Bands were detected by anti-Myc (left) or by anti-HA (right) antibodies. ( B ) Protein levels of pERK and whole ERK 10 minutes after the treatment with phenylephrine. ( C ) Summarized data of pERK/ERK (% of control) in HEK293 cells coexpressing ADRA1B-Myc and free-EGFP or ADRA1B-Myc and GPR143-EGFP ( F 1,32 = 7.899, P

    Journal: JCI Insight

    Article Title: L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor

    doi: 10.1172/jci.insight.90903

    Figure Lengend Snippet: Interaction between GPR143 and ADRA1B. ( A ) Co-immunoprecipitation (Co-IP) of ADRA1B-Myc and GPR143-HA. Bands were detected by anti-Myc (left) or by anti-HA (right) antibodies. ( B ) Protein levels of pERK and whole ERK 10 minutes after the treatment with phenylephrine. ( C ) Summarized data of pERK/ERK (% of control) in HEK293 cells coexpressing ADRA1B-Myc and free-EGFP or ADRA1B-Myc and GPR143-EGFP ( F 1,32 = 7.899, P

    Article Snippet: The sections were incubated with anti-TH (#22941, ImmunoStar) antibody, anti-GPR143 antibody , or anti-ADRA1B (#AAR-018, Alomone Labs) antibody at 4°C for 24 hours.

    Techniques: Immunoprecipitation, Co-Immunoprecipitation Assay

    Immunohistochemical staining of endogenous GPR143 and ADRA1B. Expression of GPR143 ( A ) and ADRA1B ( C ) in the liver (arrowheads). No GPR143 signals were observed in the liver of Gpr143 –/y mice ( B ). No ADRA1B signals were observed in sections incubated with the antigenic peptide–preadsorbed antibody ( D ). Scale bar: 100 μm. Endogenous interaction between GPR143 and ADRA1B. ( E ) The GPR143-ADRA1B interacting signals (green) were detected by in situ proximity ligation assay technology in WT liver (arrowheads). ( F ) No interacting signals were observed in Gpr143 –/y liver ( n = 2, independent experiments). The nucleus was counterstained by DAPI (blue). Scale bars: 5 μm.

    Journal: JCI Insight

    Article Title: L-DOPA sensitizes vasomotor tone by modulating the vascular alpha1-adrenergic receptor

    doi: 10.1172/jci.insight.90903

    Figure Lengend Snippet: Immunohistochemical staining of endogenous GPR143 and ADRA1B. Expression of GPR143 ( A ) and ADRA1B ( C ) in the liver (arrowheads). No GPR143 signals were observed in the liver of Gpr143 –/y mice ( B ). No ADRA1B signals were observed in sections incubated with the antigenic peptide–preadsorbed antibody ( D ). Scale bar: 100 μm. Endogenous interaction between GPR143 and ADRA1B. ( E ) The GPR143-ADRA1B interacting signals (green) were detected by in situ proximity ligation assay technology in WT liver (arrowheads). ( F ) No interacting signals were observed in Gpr143 –/y liver ( n = 2, independent experiments). The nucleus was counterstained by DAPI (blue). Scale bars: 5 μm.

    Article Snippet: The sections were incubated with anti-TH (#22941, ImmunoStar) antibody, anti-GPR143 antibody , or anti-ADRA1B (#AAR-018, Alomone Labs) antibody at 4°C for 24 hours.

    Techniques: Immunohistochemistry, Staining, Expressing, Mouse Assay, Incubation, In Situ, Proximity Ligation Assay