Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- RabMAb
- Advanced Validation
- 각 태그의 뜻
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Rabbit Recombinant Monoclonal SLC12A3 antibody. Carrier free. Suitable for Dot, IHC-P, WB, mIHC and reacts with Transfected cell lysate - Human, Human, Mouse, Rat samples.
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NCC, TSC, SLC12A3, Solute carrier family 12 member 3, Na-Cl cotransporter, Na-Cl symporter, Thiazide-sensitive sodium-chloride cotransporter
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human kidney tissue staining Collagen IV with ab236640 at a 1/1000 dilution, ab199975 anti-Aquaporin 2 used at 1/1000 dilution and ab316191 anti-SLC12A3 used at a 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling SLC12A3 with ab316191 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on distal tubules of human kidney (PMID : 33328404).
The section was incubated with ab316191 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
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human kidney tissue staining SLC12A3 with ab316191 at a 1/100 dilution (5.08 μg/ml), ab254222 anti-Angiotensin Converting Enzyme 1 used at a 1/4000 dilution (0.141 μg/ml) and ab199975 anti-Aquaporin 2 used at a 1/4000 dilution (0.152 μg/ml).
Panel A : merged staining of anti-SLC12A3 (green; Opal™520), anti-Angiotensin Converting Enzyme 1 (magenta; Opal™690) and anti-Aquaporin 2 (gray; Opal™570) on human kidney.
Panel B : anti-SLC12A3 staining distal tubules in human kidney.
Panel C : anti-Angiotensin Converting Enzyme 1 staining proximal tubules in human kidney.
Panel D : anti-Aquaporin 2 staining collecting tubules in human kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab316191, ab254222 and ab199975 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit using Opal Polymer HRP Ms + Rb secondary reagent. Image acquisition was performed with Leica SP8 confocal microscope.
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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling SLC12A3 with ab316191 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on human cerebrum (PMID : 8812482).
The section was incubated with ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling SLC12A3 with ab316191 at 1/100 (5.08 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on human liver (PMID : 8812482).
The section was incubated with ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on mouse cerebrum.
The section was incubated with ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on rat liver.
The section was incubated with ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 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 ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on distal tubules of mouse kidney (PMID : 26337786).
The section was incubated with ab316191 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
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded rat kidney tissue staining SLC12A3 with ab316191 at a 1/2000 dilution (0.254 μg/ml), ab254222 anti-Angiotensin Converting Enzyme 1 used at a 1/4000 dilution (0.141 μg/ml) and ab199975 anti-Aquaporin 2 used at a 1/4000 dilution (0.152 μg/ml).
Panel A : merged staining of anti-SLC12A3 (green; Opal™520), anti-Angiotensin Converting Enzyme 1 (magenta; Opal™690) and anti-Aquaporin 2 (gray; Opal™570) on rat kidney.
Panel B : anti-SLC12A3 staining distal tubules in rat kidney.
Panel C : anti-Angiotensin Converting Enzyme 1 staining proximal tubules in rat kidney.
Panel D : anti-Aquaporin 2 staining collecting tubules in rat kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab316191, ab254222 and ab199975 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit using Opal Polymer HRP Ms + Rb secondary reagent. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse kidney tissue staining Collagen IV with ab236640 at a 1/1000 dilution, ab199975 anti-Aquaporin 2 used at 1/1000 dilution and ab316191 anti-SLC12A3 used at a 1/1000 dilution.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse kidney tissue staining SLC12A3 with ab316191 at a 1/2000 dilution (0.254 μg/ml), ab254222 anti-Angiotensin Converting Enzyme 1 used at a 1/4000 dilution (0.141 μg/ml) and ab199975 anti-Aquaporin 2 used at a 1/4000 dilution (0.152 μg/ml).
Panel A : merged staining of anti-SLC12A3 (green; Opal™520), anti-Angiotensin Converting Enzyme 1 (magenta; Opal™690) and anti-Aquaporin 2 (gray; Opal™570) on mouse kidney.
Panel B : anti-SLC12A3 staining distal tubules in mouse kidney.
Panel C : anti-Angiotensin Converting Enzyme 1 staining proximal tubules in mouse kidney.
Panel D : anti-Aquaporin 2 staining collecting tubules in mouse kidney.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab316191, ab254222 and ab199975 for 30 mins at room temperature. Each round was followed by a separate fluorescent tyramide signal amplification system.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument with an Opal™ 4-color kit using Opal Polymer HRP Ms + Rb secondary reagent. Image acquisition was performed with Leica SP8 confocal microscope.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded rat kidney tissue staining Collagen IV with ab236640 at a 1/1000 dilution, ab199975 anti-Aquaporin 2 used at 1/1000 dilution and ab316191 anti-SLC12A3 used at a 1/1000 dilution.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on rat cerebrum.
The section was incubated with ab316191 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-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling SLC12A3 with ab316191 at 1/2000 (0.254 ug/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on distal tubules of rat kidney (PMID : 21865292).
The section was incubated with ab316191 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.
- WB
Supplier Data
Western blot - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Negative control : lung (PMID : 35591852), liver (PMID : 35591852).
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) staining at 1/200000 dilution.
All lanes:
Western blot - Anti-SLC12A3 antibody [EPR27106-48] (<a href='/ko/products/primary-antibodies/slc12a3-antibody-epr27106-48-ab316191'>ab316191</a>) at 1/1000 dilution
Lane 1:
Mouse kidney tissue lysate at 20 µg
Lane 2:
Mouse liver tissue lysate at 20 µg
Lane 3:
Mouse lung tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/ko/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/2000 dilution
Observed band size: 150 kDa,36 kDa
false
Exposure time: 180s
- Dot
Supplier Data
Dot Blot - Anti-SLC12A3 antibody [EPR27106-48] - BSA and Azide free (AB316192)
This data was developed using ab316191, the same antibody clone in a different buffer formulation.
Dot blot analysis of SLC12A3 using ab316191 at 1 : 1000 (0.508 ug/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with human SLC12A1 and human SLC12A2.
All lanes:
Dot Blot - Anti-SLC12A3 antibody [EPR27106-48] (<a href='/ko/products/primary-antibodies/slc12a3-antibody-epr27106-48-ab316191'>ab316191</a>) at 1/1000 dilution
Lane 1:
293T cells transfected with an empty vector containing a His-tag, whole cell lysate at 10 µg
Lane 2:
293T cells transfected with a SLC12A3 expression vector containing a His-tag, whole cell lysate at 10 µg
Lane 3:
293T cells transfected with a SLC12A1 expression vector containing a His-tag, whole cell lysate at 10 µg
Lane 4:
293T cells transfected with a SLC12A2 expression vector containing a His-tag, whole cell lysate at 10 µg
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: 169s
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-SLC12A3 antibody [EPR27106-48]
Reactivity 정보
제품 세부 정보
ab316192 is the carrirer-free version of ab316191.
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.
Conjugation ready
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
Compatibility
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
특성 및 보관 정보
제형
Purification 테크닉
보관 버퍼
배송 시 보관 조건
적절한 단기 보관 조건
적절한 장기 보관 조건
추가 정보
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The activity of SLC12A3 regulates blood pressure and volume homeostasis. It is an integral part of ion transport mechanisms and operates within a network of other transporters and channels in the kidney. The proper function of this transporter balances sodium and chloride reabsorption preventing excessive loss or retention. While not directly forming a complex its activity correlates with the function of other ion transport proteins in maintaining ion balance.
Pathways
The SLC12A3 protein integrates into the renal system's regulation of electrolyte homeostasis. It interacts within the salt-sensitive pathway by influencing the reabsorption of sodium chloride which impacts the renin-angiotensin-aldosterone system (RAAS) indirectly. The activity of SLC12A3 influences blood pressure regulation connecting it functionally with proteins like WNK kinases which modulate its phosphorylation state altering its transport capacity.
제품 프로토콜
- Visit the General protocols
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타겟 정보
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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