Anti-SGLT1 antibody [EPR26041-107] - BSA and Azide free
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- BOND RX™ Validated
- Recombinant
- RabMAb
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- mIHC
Lab
Multiplex immunohistochemistry - Anti-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human small intestine staining SGLT1 with ab321787 at a 1/2000 dilution, ab272692 anti-MUS2 used at 1/2000 dilution and ab252935 anti-EPHB2 used at a 1/500 dilution.
Panel A : merged staining of anti-SGLT1 (green; Opal™520), anti-MUC2 (magenta; Opal™690) and anti-EPHB2 (gray; Opal™570) on human small intestine.
Panel B : anti-SGLT2 staining apical side of the villi in human small intestine.
Panel C : anti-MUC2 staining goblet cells in human small intestine.
Panel D : anti-EPHB2 staining stem cells in human small intestine.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab321787, ab272692 and ab252935 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. Image acquisition was performed with Leica SP8 confocal microscope.
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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human skeletal muscle tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on human skeletal muscle.
The section was incubated with ab321787 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
We don't expect this antibody to cross-react with SGLT3 (SLC5A4) based on the negative staining observed in skeletal muscle which expresses SGLT3 (PMID : 33385407).
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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded (A) HEK-293T (human embryonic kidney epithelial cell) transfected with a SGLT1 (SLC5A1) expression vector containing a his tag. (B) HEK-293T cells transfected with a SGLT2 (SLC5A2) expression vector containing a his tag. (C) HEK-293T cells transfected with empty vector containing a his tag. tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) HEK-293T cells transfected with a SGLT1 (SLC5A1) expression vector containing a his tag No staining on (B) HEK-293T cells transfected with a SGLT2 (SLC5A2) expression vector and (C) HEK-293T cells transfected with empty vector containing a his tag.
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded human kidney tissue staining CD34 with ab317588 at a 1/2000 dilution, ab321787 anti-SGLT1 used at 1/2000 dilution and ab212197 anti-Renin used at a 1/4000 dilution.
Panel A : merged staining of anti-CD34 (green; Opal™520), anti-SGLT1 (magenta; Opal™690) and anti-Renin (gray; Opal™570) on human kidney.
Panel B : anti-CD34 staining endothelium in human kidney.
Panel C : anti-SGLT1 staining tubules in human kidney.
Panel D : anti-Renin staining juxtaglomerular cells 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 ab317588, ab321787 and ab212197 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. Image acquisition was performed with Leica SP8 confocal microscope.
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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human kidney (PMID : 26121582).
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human duodenum tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human duodenum.
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on human cerebrum.
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on rat skeletal muscle.
The section was incubated with ab321787 for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument
We don't expect this antibody to cross-react with SGLT3 (SLC5A4) based on the negative staining observed in skeletal muscle which expresses SGLT3 (PMID : 33385407).
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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control : No staining on rat cerebrum (PMID : 8163506).
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat kidney.
The section was incubated with ab321787 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-SGLT1 antibody [EPR26041-107] - BSA and Azide free (AB321788)
This data was developed using ab321787, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat duodenum tissue labeling SGLT1 with ab321787 at 1/2000 (0.268 ug/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat duodenum (PMID : 8163506).
The section was incubated with ab321787 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
관련 conjugated 항체와 다양한 조성의 항체 (1)
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Anti-SGLT1 antibody [EPR26041-107]
Reactivity 정보
제품 세부 정보
ab321788 is the carrier-free version of ab321787.
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.
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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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