Anti-Mu Opioid Receptor antibody [EPR29112-126]
- BOND RX™ Validated
- Advanced Validation
- RabMAb
- Recombinant
- 20ul selling size
- 각 태그의 뜻
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- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse spinal cord tissue staining Mu Opioid Receptor with ab323645 at a 1 : 2000 (0.252 ug/ml) dilution, ab307138 anti-TAC1 used at 1 : 500 (0.966 ug/ml) dilution and ab316105 anti-GPCR GPR17 used at a 1 : 500 (0.509ug/ml) dilution.
Panel A : merged staining of anti-OPRM1 (magenta; Opal™520), anti-TAC1 (green; Opal™690) and anti-GPCR GPR17 (yellow; Opal™570) on mouse spinal cord.
Panel B : anti-OPRM1 showed positive staining in mouse spinal cord.
Panel C : anti-TAC1 showed positive staining in mouse spinal cord.
Panel D : anti-GPCR GPR17 staining oligodendrocytes in mouse spinal cord.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab323645, ab307138 and ab316105 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
Nuclear counter stain with DAPI.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat liver (PMID : 7605935). The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse liver. The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on mouse spleen. The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat cerebrum. The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Rat spinal cord tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat spinal cord (PMID : 32723769; PMID : 29473323). The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded rat spinal cord tissue staining Mu Opioid Receptor with ab323645 at a 1 : 2000 (0.252 ug/ml) dilution, ab307138 anti-TAC1 used at 1 : 500 (0.966 ug/ml) dilution and ab316105 anti-GPCR GPR17 used at a 1 : 500 (0.509ug/ml) dilution.
Panel A : merged staining of anti-OPRM1 (magenta; Opal™520), anti-TAC1 (green; Opal™690) and anti-GPCR GPR17 (yellow; Opal™570) on rat spinal cord.
Panel B : anti-OPRM1 showed positive staining in rat spinal cord.
Panel C : anti-TAC1 showed positive staining in rat spinal cord.
Panel D : anti-GPCR GPR17 staining oligodendrocytes in rat spinal cord.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab323645, ab307138 and ab316105 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
Nuclear counter stain with DAPI.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse cerebrum (PMID : 11717463). The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : no staining on rat spleen. The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Immunohistochemical analysis of paraffin-embedded Mouse spinal cord tissue labeling Mu Opioid Receptor with ab323645 at 1/2000 (0.252 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse spinal cord (PMID : 11717463). The section was incubated with ab323645 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
Counterstained with Hematoxylin.
Secondary antibody only control : Secondary antibody is a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins
- Dot
Supplier Data
Dot Blot - Anti-Mu Opioid Receptor antibody [EPR29112-126] (AB323645)
Dot blot analysis of Mu Opioid Receptor using ab323645 at 1 : 1000 (0.504 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane1 : 293T cells transfected with a mouse Mu Opioid Receptor expression vector containing a His-tag, whole cell lysate
Exposure time : 180 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Dot Blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) staining at 1/5000 dilution.
All lanes:
Dot Blot - Anti-Mu Opioid Receptor antibody [EPR29112-126] (ab323645) at 1/1000 dilution
All lanes:
293T cells transfected with a mouse Mu Opioid Receptor expression vector containing a His-tag, whole cell lysate
Secondary
All lanes:
Dot Blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
false
Exposure time: 180s
Reactivity 정보
제품 세부 정보
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free batch production
For more information, read more on recombinant antibodies.
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Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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