Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- Advanced Validation
- RabMAb
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Rabbit Recombinant Monoclonal Noradrenaline transporter antibody. Carrier free. Suitable for mIHC, Flow Cyt, WB, IHC-P, IHC-Fr and reacts with Mouse, Rat, Human samples.
View Alternative Names
NAT1, NET1, SLC6A5, SLC6A2, Sodium-dependent noradrenaline transporter, Norepinephrine transporter, Solute carrier family 6 member 2, NET
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labelling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab254361 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Positive staining in human cerebrum.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab254361).
Multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded human cerebrum tissue section labelling Noradrenaline transporter with ab254361 at a 1/100 dilution (B), GPCR GPR17 with ab314307 at a 1/500 dilution (C), and ARMET/ARP with ab316935 at a 1/1000 dilution (D). Nuclear DNA was labeled with DAPI (shown in blue).
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™ 690), anti-GPCR GPR17 (green; Opal™ 520) and anti-ARMET/ARP (gray; Opal™ 570) on human cerebrum.
Panel B : anti-Noradrenaline transporter staining nerves in human cerebrum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in human cerebrum.
Panel D : anti-ARMET/ARP staining neurons in human cerebrum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab316935 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat liver tissue labelling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab254361 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Negative control : no staining in rat hepatocytes.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
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-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse liver tissue labelling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab254361 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Negative control : no staining in mouse hepatocytes.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- Flow Cyt
Supplier Data
Flow Cytometry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of rat primary neuron cells labelling Noradrenaline transporter with ab254361 at 1/50 dilution (1μg)/ Right compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control. Goat anti rabbit IgG (Alexa Fluor® 647, ab150079) at 1/2000 dilution was used as the secondary antibody.
Gated on viable cells.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labelling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab254361 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Positive staining in rat cerebrum.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat cerebrum tissue labeling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
Positive staining on rat cerebrum is observed.
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse cerebrum tissue labeling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
Positive staining on mouse cerebrum is observed.
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat liver tissue labeling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
Negative control : No staining on rat liver (PMID : 12807698) is observed.
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse cerebellum labelling Noradrenaline transporter with ab254361 at 1/100 (B), GPCR GPR17 with ab314307 at 1/2000 dilution (C) and FMRP with ab259335 at 1/10000 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and Nuclear DNA was labeled with DAPI (shown in blue). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™690), anti-GPCR GPR17 (green; Opal™520) and anti-FMRP (gray; Opal™570) on mouse cerebellum.
Panel B : anti-Noradrenaline transporter staining nerves in mouse cerebellum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in mouse cerebellum.
Panel D : anti-FMRP staining neurons in mouse cerebellum.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab259335 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.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse cerebrum labelling Noradrenaline transporter with ab254361 at 1/100 (B), GPCR GPR17 with ab314307 at 1/2000 dilution (C) and FMRP with ab259335 at 1/10000 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and Nuclear DNA was labeled with DAPI (shown in blue). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™690), anti-GPCR GPR17 (green; Opal™520) and anti-FMRP (gray; Opal™570) on mouse cerebrum.
Panel B : anti-Noradrenaline transporter staining nerves in mouse cerebrum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in mouse cerebrum.
Panel D : anti-FMRP staining neurons in mouse cerebrum.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab259335 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.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat cerebellum labelling Noradrenaline transporter with ab254361 at 1/100 (B), GPCR GPR17 with ab314307 at 1/2000 dilution (C) and FMRP with ab259335 at 1/10000 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and Nuclear DNA was labeled with DAPI (shown in blue). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™690), anti-GPCR GPR17 (green; Opal™520) and anti-FMRP (gray; Opal™570) on rat cerebellum.
Panel B : anti-Noradrenaline transporter staining nerves in rat cerebellum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in rat cerebellum.
Panel D : anti-FMRP staining neurons in rat cerebellum.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab259335 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.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat cerebrum labelling Noradrenaline transporter with ab254361 at 1/100 (B), GPCR GPR17 with ab314307 at 1/2000 dilution (C) and FMRP with ab259335 at 1/10000 dilution (D). Opal Polymer HRP Ms + Rb was used as a secondary antibody, and Nuclear DNA was labeled with DAPI (shown in blue). Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™690), anti-GPCR GPR17 (green; Opal™520) and anti-FMRP (gray; Opal™570) on rat cerebrum.
Panel B : anti-Noradrenaline transporter staining nerves in rat cerebrum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in rat cerebrum.
Panel D : anti-FMRP staining neurons in rat cerebrum.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab259335 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.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab254361).
Multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebellum tissue section labelling Noradrenaline transporter with ab254361 at a 1/100 dilution (B), GPCR GPR17 with ab314307 at a 1/2000 dilution (C), and ARMET/ARP with ab316935 at a 1/20000 dilution (D). Nuclear DNA was labeled with DAPI (shown in blue).
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™ 690), anti-GPCR GPR17 (green; Opal™ 520) and anti-ARMET/ARP (gray; Opal™ 570) on mouse cerebellum.
Panel B : anti-Noradrenaline transporter staining nerves in mouse cerebellum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in mouse cerebellum.
Panel D : anti-ARMET/ARP staining neurons in mouse cerebellum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab316935 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.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labelling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection). The section was incubated with ab254361 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Positive staining in mouse cerebrum.
Secondary antibody only control : Secondary antibody is ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab254361).
Multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat cerebellum tissue section labelling Noradrenaline transporter with ab254361 at a 1/100 dilution (B), GPCR GPR17 with ab314307 at a 1/2000 dilution (C), and ARMET/ARP with ab316935 at a 1/20000 dilution (D). Nuclear DNA was labeled with DAPI (shown in blue).
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™ 690), anti-GPCR GPR17 (green; Opal™ 520) and anti-ARMET/ARP (gray; Opal™ 570) on rat cerebellum.
Panel B : anti-Noradrenaline transporter staining nerves in rat cerebellum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in rat cerebellum.
Panel D : anti-ARMET/ARP staining neurons in rat cerebellum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab316935 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.
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab254361).
Multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded rat cerebrum tissue section labelling Noradrenaline transporter with ab254361 at a 1/100 dilution (B), GPCR GPR17 with ab314307 at a 1/2000 dilution (C), and ARMET/ARP with ab316935 at a 1/20000 dilution (D). Nuclear DNA was labeled with DAPI (shown in blue).
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™ 690), anti-GPCR GPR17 (green; Opal™ 520) and anti-ARMET/ARP (gray; Opal™ 570) on rat cerebrum.
Panel B : anti-Noradrenaline transporter staining nerves in rat cerebrum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in rat cerebrum.
Panel D : anti-ARMET/ARP staining neurons in rat cerebrum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab316935 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.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse liver tissue labeling Noradrenaline transporter with ab254361 at 1/100 (5.33 μg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). The nuclear counterstain was DAPI (Blue).
Negative control : No staining on mouse liver (PMID : 12807698) is observed.
Secondary antibody control : Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
- mIHC
Supplier Data
Multiplex immunohistochemistry - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab254361).
Multiplex immunohistochemical analysis of formalin/PFA-fixed paraffin-embedded mouse cerebrum tissue section labelling Noradrenaline transporter with ab254361 at a 1/100 dilution (B), GPCR GPR17 with ab314307 at a 1/2000 dilution (C), and ARMET/ARP with ab316935 at a 1/20000 dilution (D). Nuclear DNA was labeled with DAPI (shown in blue).
Panel A : merged staining of anti-Noradrenaline transporter (magenta; Opal™ 690), anti-GPCR GPR17 (green; Opal™ 520) and anti-ARMET/ARP (gray; Opal™ 570) on mouse cerebrum.
Panel B : anti-Noradrenaline transporter staining nerves in mouse cerebrum.
Panel C : anti-GPCR GPR17 staining oligodendrocytes in mouse cerebrum.
Panel D : anti-ARMET/ARP staining neurons in mouse cerebrum.
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
The section was incubated in three rounds of staining : in the order of ab254361, ab314307 and ab316935 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.
- WB
Lab
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Negative control : 293T. In Western blot, anti-Vinculin antibody (ab129002) staining at 1/10, 000 dilution. Samples are non-boiled as boiling may cause protein aggregation.
All lanes:
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] (<a href='/en-us/products/primary-antibodies/noradrenaline-transporter-antibody-epr23527-534-ab254361'>ab254361</a>) at 1/1000 dilution
Lane 1:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
Lane 2:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 69 kDa
Observed band size: 69 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
In Western blot, anti-GAPDH antibody (ab181602) staining at 1/200,000 dilution and anti-Integrin alpha V (ab179475) staining at 1/5,000 dilution.
Samples are non-boiled as boiling may cause protein aggregation.
All lanes:
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] (<a href='/en-us/products/primary-antibodies/noradrenaline-transporter-antibody-epr23527-534-ab254361'>ab254361</a>) at 1/1000 dilution
Lane 1:
Mouse brain membrane tissue lysate at 20 µg
Lane 2:
Mouse membrane-depleted tissue lysate at 20 µg
Lane 3:
Rat brain membrane tissue lysate at 20 µg
Lane 4:
Rat membrane-depleted tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 69 kDa
Observed band size: 69 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] - BSA and Azide free (AB282022)
This data was developed using ab254361, the same antibody clone in a different buffer formulation. Blocking and diluting buffer and concentration : 5% NFDM/TBST. Negative control : mouse skeletal muscle and rat liver. In Western blot, anti-GAPDH antibody (ab181602) was used as a GAPDH loading control and staining at 1/200, 000 dilution. Samples are non-boiled as boiling may cause protein aggregation
All lanes:
Western blot - Anti-Noradrenaline transporter antibody [EPR23527-534] (<a href='/en-us/products/primary-antibodies/noradrenaline-transporter-antibody-epr23527-534-ab254361'>ab254361</a>) at 1/1000 dilution
Lane 1:
Mouse cerebral cortex tissue lysate at 20 µg
Lane 2:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 3:
Rat brain tissue lysate at 20 µg
Lane 4:
Rat dorsal ganglion tissue lysate at 20 µg
Lane 5:
Rat liver tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Predicted band size: 69 kDa
Observed band size: 69 kDa
false
Exposure time: 180s
Related conjugates and formulations (1)
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Anti-Noradrenaline transporter antibody [EPR23527-534]
Reactivity data
Product details
ab282022 is the carrier-free version of ab254361.
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
The noradrenaline transporter functions to regulate extracellular levels of noradrenaline which is essential for proper functioning of the sympathetic nervous system. It is vital in the reuptake mechanism that controls the duration and intensity of noradrenaline's action. The transporter forms part of a larger complex that involves various proteins and binding molecules that facilitate noradrenaline reuptake efficiently by ensuring synaptic concentration of needed ions.
Pathways
The activity of the noradrenaline transporter is an integral part of the adrenergic signaling pathway which is instrumental in the body's response to stress. This pathway includes complex interactions involving G protein-coupled receptors and proteins like dopamine transporter which sometimes parallel its action. The transporter is also involved in the catecholamine biosynthesis pathway which is responsible for the production and breakdown of neurotransmitters including adrenaline and dopamine.
Product protocols
- Visit the General protocols
- Visit the Troubleshooting
Target data
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
For licensing inquiries, please contact partnerships@abcam.com