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rabbit anti cb2  (Danaher Inc)


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    Structured Review

    Danaher Inc rabbit anti cb2
    qPCR evaluation of the cannabinoid receptor expression in the model cell lines. HL60 and LN229 cell lines were used as a reference with a high expression of <t>CB2</t> and CB1 and GPR55 receptor pair, accordingly.
    Rabbit Anti Cb2, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+cb2/pmc10888638-162-9-11
    Average 86 stars, based on 1 article reviews
    rabbit anti cb2 - by Bioz Stars, 2026-10
    86/100 stars

    Images

    1) Product Images from "The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells"

    Article Title: The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells

    Journal: International Journal of Molecular Sciences

    doi: 10.3390/ijms25042271

    qPCR evaluation of the cannabinoid receptor expression in the model cell lines. HL60 and LN229 cell lines were used as a reference with a high expression of CB2 and CB1 and GPR55 receptor pair, accordingly.
    Figure Legend Snippet: qPCR evaluation of the cannabinoid receptor expression in the model cell lines. HL60 and LN229 cell lines were used as a reference with a high expression of CB2 and CB1 and GPR55 receptor pair, accordingly.

    Techniques Used: Expressing

    The effect of receptor blockers on the effect of AEA’s combination with LPI on breast cancer cell lines’ viability. The following substances and concentrations were used: CB1, SR 141716A (100 nM); CB2, SR 144528 (100 nM); GPR55, ML-193 (2 µM); GPR18, PSB CB5 (3 µM). Incubation time: 72 h; resazurin test, mean ± standard error ( n = 4 experiments). ( A ) MCF-10A, ( B ) MCF-7, ( C ) BT-474, ( D ) SK-BR-3, ( E ) BT-20, ( F ) MDA-MB-231.
    Figure Legend Snippet: The effect of receptor blockers on the effect of AEA’s combination with LPI on breast cancer cell lines’ viability. The following substances and concentrations were used: CB1, SR 141716A (100 nM); CB2, SR 144528 (100 nM); GPR55, ML-193 (2 µM); GPR18, PSB CB5 (3 µM). Incubation time: 72 h; resazurin test, mean ± standard error ( n = 4 experiments). ( A ) MCF-10A, ( B ) MCF-7, ( C ) BT-474, ( D ) SK-BR-3, ( E ) BT-20, ( F ) MDA-MB-231.

    Techniques Used: Incubation

    Related Articles

    Expressing:

    Article Title: The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells
    Article Snippet: Proteins were separated using denaturing SDS-PAGE in 10% gel with the PageRuler protein ladder (Thermo Fisher Scientific, Waltham, MA USA), transferred to a nitrocellulose membrane using the Invitrogen Power Blotter with the Invitrogen Power Blotter 1-step transfer buffer (Thermo Fisher Scientific, Waltham, MA USA) and Invitrogen precut membranes and filters (Thermo Fisher Scientific, Waltham, MA USA), and stained with antibodies using the Invitrogen iBind system (Thermo Fisher Scientific, Waltham, MA USA) according to the manufacturer’s protocol.

    Incubation:

    Article Title: The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells
    Article Snippet: Proteins were separated using denaturing SDS-PAGE in 10% gel with the PageRuler protein ladder (Thermo Fisher Scientific, Waltham, MA USA), transferred to a nitrocellulose membrane using the Invitrogen Power Blotter with the Invitrogen Power Blotter 1-step transfer buffer (Thermo Fisher Scientific, Waltham, MA USA) and Invitrogen precut membranes and filters (Thermo Fisher Scientific, Waltham, MA USA), and stained with antibodies using the Invitrogen iBind system (Thermo Fisher Scientific, Waltham, MA USA) according to the manufacturer’s protocol.



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    Fig. 1. Immunohistochemistry for CB1 and <t>CB2</t> in the carotid body. (A) Dot-like CB1 immunoreactivity is observed throughout the carotid body. Intense immu- noreactivity is shown in nerve fibers and/or endings (arrows). (B) A higher magnification view of the rectangle in panel A. Dot-like CB1 immunoreactivity is observed in the perinuclear cytoplasm of chemoreceptor cells (arrows). Intense immunoreactivity for CB1 is also present in nerve endings (arrowheads). (C) Dot-like CB2 immunoreactivity is noted throughout the carotid body. (D) A higher magnification view (rectangle in panel C) shows small dots of CB2 immunoreactivity in the perinuclear region of chemoreceptor cells (arrow). (E-G) Double immunofluorescence for CB1 and CB2 shows CB1-immunoreactive (arrows) and CB2- immunoreactive dots (arrow heads) in the same chemoreceptor cell; however, they are not colocalized.
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    Image Search Results


    Fig. 1. Immunohistochemistry for CB1 and CB2 in the carotid body. (A) Dot-like CB1 immunoreactivity is observed throughout the carotid body. Intense immu- noreactivity is shown in nerve fibers and/or endings (arrows). (B) A higher magnification view of the rectangle in panel A. Dot-like CB1 immunoreactivity is observed in the perinuclear cytoplasm of chemoreceptor cells (arrows). Intense immunoreactivity for CB1 is also present in nerve endings (arrowheads). (C) Dot-like CB2 immunoreactivity is noted throughout the carotid body. (D) A higher magnification view (rectangle in panel C) shows small dots of CB2 immunoreactivity in the perinuclear region of chemoreceptor cells (arrow). (E-G) Double immunofluorescence for CB1 and CB2 shows CB1-immunoreactive (arrows) and CB2- immunoreactive dots (arrow heads) in the same chemoreceptor cell; however, they are not colocalized.

    Journal: Acta histochemica

    Article Title: Immunohistochemical distribution of cannabinoid receptor type 1 (CB1) and type 2 (CB2) in the rat carotid body.

    doi: 10.1016/j.acthis.2024.152205

    Figure Lengend Snippet: Fig. 1. Immunohistochemistry for CB1 and CB2 in the carotid body. (A) Dot-like CB1 immunoreactivity is observed throughout the carotid body. Intense immu- noreactivity is shown in nerve fibers and/or endings (arrows). (B) A higher magnification view of the rectangle in panel A. Dot-like CB1 immunoreactivity is observed in the perinuclear cytoplasm of chemoreceptor cells (arrows). Intense immunoreactivity for CB1 is also present in nerve endings (arrowheads). (C) Dot-like CB2 immunoreactivity is noted throughout the carotid body. (D) A higher magnification view (rectangle in panel C) shows small dots of CB2 immunoreactivity in the perinuclear region of chemoreceptor cells (arrow). (E-G) Double immunofluorescence for CB1 and CB2 shows CB1-immunoreactive (arrows) and CB2- immunoreactive dots (arrow heads) in the same chemoreceptor cell; however, they are not colocalized.

    Article Snippet: CB2: A rabbit polyclonal anti-CB2 antibody (NB300–606, Novus Biologicals, Centennial, CO, U.S.A.) was raised from a fusion protein that contained the first 33 amino acid residues of human CB2.

    Techniques: Immunohistochemistry, Immunofluorescence

    Fig. 2. (A-C)Triple immunofluorescence for CB1 with TH and DBH. CB1-immunoreactive dot-like structures are observed in both TH- (arrows) and DBH- immunoreactive chemoreceptor cells (arrowheads). Dot-like immunoreactivity for CB1 localizes in both the perinuclear cytoplasm and outlines of the regions of immunoreactivity for TH or DBH. (D-F) Triple immunofluorescence for CB2 with TH and DBH. CB2 immunoreactivity is shown in the perinuclear cytoplasm of TH- (arrows) and DBH-immunoreactive chemoreceptor cells (arrowheads).

    Journal: Acta histochemica

    Article Title: Immunohistochemical distribution of cannabinoid receptor type 1 (CB1) and type 2 (CB2) in the rat carotid body.

    doi: 10.1016/j.acthis.2024.152205

    Figure Lengend Snippet: Fig. 2. (A-C)Triple immunofluorescence for CB1 with TH and DBH. CB1-immunoreactive dot-like structures are observed in both TH- (arrows) and DBH- immunoreactive chemoreceptor cells (arrowheads). Dot-like immunoreactivity for CB1 localizes in both the perinuclear cytoplasm and outlines of the regions of immunoreactivity for TH or DBH. (D-F) Triple immunofluorescence for CB2 with TH and DBH. CB2 immunoreactivity is shown in the perinuclear cytoplasm of TH- (arrows) and DBH-immunoreactive chemoreceptor cells (arrowheads).

    Article Snippet: CB2: A rabbit polyclonal anti-CB2 antibody (NB300–606, Novus Biologicals, Centennial, CO, U.S.A.) was raised from a fusion protein that contained the first 33 amino acid residues of human CB2.

    Techniques: Immunofluorescence

    Fig. 3. (A-C) Double immunofluorescence for CB1 with P2X3. Intense CB1 immunoreactivity is surrounded by P2X3 immunoreactivity in the sensory nerve endings around chemoreceptor cells (arrows). (D-F) Double immunofluorescence for CB1 with VGluT2. CB1 immunoreactivity colocalizes with VGluT2 immunoreactivity, and appears to be in close contact with chemoreceptor cells (arrows). (G-H) Double immunofluorescence for CB2 with P2X2. Weak CB2-immunoreactive dots localize within P2X2-immunoreactive sensory nerve endings (arrows).

    Journal: Acta histochemica

    Article Title: Immunohistochemical distribution of cannabinoid receptor type 1 (CB1) and type 2 (CB2) in the rat carotid body.

    doi: 10.1016/j.acthis.2024.152205

    Figure Lengend Snippet: Fig. 3. (A-C) Double immunofluorescence for CB1 with P2X3. Intense CB1 immunoreactivity is surrounded by P2X3 immunoreactivity in the sensory nerve endings around chemoreceptor cells (arrows). (D-F) Double immunofluorescence for CB1 with VGluT2. CB1 immunoreactivity colocalizes with VGluT2 immunoreactivity, and appears to be in close contact with chemoreceptor cells (arrows). (G-H) Double immunofluorescence for CB2 with P2X2. Weak CB2-immunoreactive dots localize within P2X2-immunoreactive sensory nerve endings (arrows).

    Article Snippet: CB2: A rabbit polyclonal anti-CB2 antibody (NB300–606, Novus Biologicals, Centennial, CO, U.S.A.) was raised from a fusion protein that contained the first 33 amino acid residues of human CB2.

    Techniques: Immunofluorescence

    qPCR evaluation of the cannabinoid receptor expression in the model cell lines. HL60 and LN229 cell lines were used as a reference with a high expression of CB2 and CB1 and GPR55 receptor pair, accordingly.

    Journal: International Journal of Molecular Sciences

    Article Title: The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells

    doi: 10.3390/ijms25042271

    Figure Lengend Snippet: qPCR evaluation of the cannabinoid receptor expression in the model cell lines. HL60 and LN229 cell lines were used as a reference with a high expression of CB2 and CB1 and GPR55 receptor pair, accordingly.

    Article Snippet: The following antibodies were used: rabbit anti-GPR55 (Abcam ab203663), rabbit anti-CB2 (Abcam ab45942), rabbit anti-CB1 (Abcam ab23703), and mouse anti-beta-actin (Abcam ab8226); and secondary antibodies (coupled to alkaline phosphatase) anti-rabbit IgG (Sigma-Aldrich A9919) and anti-mouse IgG (Jackson ImmunoResearch 111-055-003).

    Techniques: Expressing

    The effect of receptor blockers on the effect of AEA’s combination with LPI on breast cancer cell lines’ viability. The following substances and concentrations were used: CB1, SR 141716A (100 nM); CB2, SR 144528 (100 nM); GPR55, ML-193 (2 µM); GPR18, PSB CB5 (3 µM). Incubation time: 72 h; resazurin test, mean ± standard error ( n = 4 experiments). ( A ) MCF-10A, ( B ) MCF-7, ( C ) BT-474, ( D ) SK-BR-3, ( E ) BT-20, ( F ) MDA-MB-231.

    Journal: International Journal of Molecular Sciences

    Article Title: The Interaction of the Endocannabinoid Anandamide and Paracannabinoid Lysophosphatidylinositol during Cell Death Induction in Human Breast Cancer Cells

    doi: 10.3390/ijms25042271

    Figure Lengend Snippet: The effect of receptor blockers on the effect of AEA’s combination with LPI on breast cancer cell lines’ viability. The following substances and concentrations were used: CB1, SR 141716A (100 nM); CB2, SR 144528 (100 nM); GPR55, ML-193 (2 µM); GPR18, PSB CB5 (3 µM). Incubation time: 72 h; resazurin test, mean ± standard error ( n = 4 experiments). ( A ) MCF-10A, ( B ) MCF-7, ( C ) BT-474, ( D ) SK-BR-3, ( E ) BT-20, ( F ) MDA-MB-231.

    Article Snippet: The following antibodies were used: rabbit anti-GPR55 (Abcam ab203663), rabbit anti-CB2 (Abcam ab45942), rabbit anti-CB1 (Abcam ab23703), and mouse anti-beta-actin (Abcam ab8226); and secondary antibodies (coupled to alkaline phosphatase) anti-rabbit IgG (Sigma-Aldrich A9919) and anti-mouse IgG (Jackson ImmunoResearch 111-055-003).

    Techniques: Incubation