Anti-Plasmolipin antibody [EPR31074-536]
- RabMAb
- Recombinant
- 20ul selling size
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Rabbit Recombinant Monoclonal PLLP antibody. Suitable for Dot, IHC-Fr, ICC/IF, IHC-P, WB and reacts with Synthetic peptide - Human, Mouse, Rat, Human samples.
View Alternative Names
PMLP, TM4SF11, PLLP, Plasmolipin, Plasma membrane proteolipid
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Human sciatic nerve tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human sciatic nerve.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Human liver tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on human liver.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human kidney.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Human cerebrum tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on human cererbrum.
The primary antibody was incubated 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
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized BxPC-3 (human pancreas adenocarcinoma epithelial cell) and U-937 (human histiocytic lymphoma monocyte) cells labelling Plasmolipin with ab325932 at 1/50 (10.0 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in BxPC-3 cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Low expression : U-937.
ab7291 Anti-alpha Tubulin mouse monoclonal antibody was used to counterstain tubulin at 1/1000 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab325932 at 1/50 dilution, followed by ab150120 at 1/1000 dilution.
-ve control 2 : ab7291 at 1/1000 dilution, followed by ab150081 at 1/1000 dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse kidney.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Mouse spleen tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on mouse spleen.
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Rat spleen tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression tissue : No staining on rat spleen (PMID : 8714710).
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Mouse sciatic nerve tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse sciatic nerve.
The primary antibody was incubated 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-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse spleen (fresh frozen) tissue labeling Plasmolipin with ab325932 at 1/500 (1.0 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green).
Low expression : confocal image showing no staining on mouse spleen. The nuclear counterstain was DAPI (Blue). The section was incubated with ab305372 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Rat sciatic nerve tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat sciatic nerve (PMID : 8714710).
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat kidney (PMID : 12871592).
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Rat brain (Coronal section) tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on rat brain. (A) Low-powered (magnification, x20) and (B) high-powered (magnification, x200) microscopic images (PMID : 12871592).
The primary antibody was incubated 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
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of paraffin-embedded Mouse brain (Coronal section) tissue labeling Plasmolipin with ab325932 at 1/2000 (0.25 µg/ml) dilution, followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on mouse brain. (A) Low-powered (magnification, x20) and (B) high-powered (magnification, x200) microscopic images.
The primary antibody was incubated 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
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary oligodendrocyte cells labelling Plasmolipin with ab325932 at 1/50 (10.0 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in mouse primary oligodendrocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-Myelin Basic Protein rat monoclonal antibody was used to counterstain tubulin at 1/200 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab325932 at 1/50 dilution, followed by ab150160 at 1/1000 dilution.
-ve control 2 : Anti-Myelin Basic Protein rat monoclonal antibody at 1/200 dilution, followed by ab150081 at 1/1000 dilution.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat spleen (fresh frozen) tissue labeling Plasmolipin with ab325932 at 1/500 (1.0 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green).
Low expression : confocal image showing no staining on rat spleen (PMID : 8714710). The nuclear counterstain was DAPI (Blue). The section was incubated with ab305372 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse cerebellum (fresh frozen) tissue labeling Plasmolipin with ab325932 at 1/500 (1.0 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green).
Panel A : merged staining of anti-PLLP (ab325932, green), anti-MOG (ab305372, magenta) on mouse cerebellum.
Panel B : anti-PLLP stained on mouse cerebellum.
Panel C : anti-MOG stained in myelin of mouse cerebellum.
The section was incubated in two rounds of staining : in the order of ab325932 and ab305372, for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Rat cerebellum (fresh frozen) tissue labeling Plasmolipin with ab325932 at 1/500 (1.0 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution (Green).
Panel A : merged staining of anti-PLLP (ab325932, green), anti-MOG (ab305372, magenta) on rat cerebellum.
Panel B : anti-PLLP stained on rat cerebellum.
Panel C : anti-MOG stained in myelin of rat cerebellum.
The section was incubated in two rounds of staining : in the order of ab325932 and ab305372, for 1 hr at room temperature. The nuclear counterstain was DAPI (Blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat splenocyte cells labelling Plasmolipin with ab325932 at 1/50 (10.0 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Low expression : confocal image showing no staining in rat splenocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-rat CD3 mouse monoclonal antibody (Alexa Fluor® 647) was used to counterstain tubulin at 1/100 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat primary oligodendrocyte cells labelling Plasmolipin with ab325932 at 1/50 (10.0 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Confocal image showing cytoplasmic staining in rat primary oligodendrocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-Myelin Basic Protein rat monoclonal antibody was used to counterstain tubulin at 1/200 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1 : ab325932 at 1/50 dilution, followed by ab150160 at 1/1000 dilution.
-ve control 2 : Anti-Myelin Basic Protein rat monoclonal antibody at 1/200 dilution, followed by ab150081 at 1/1000 dilution.
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse splenocyte cells labelling Plasmolipin with ab325932 at 1/50 (10.0 µg/ml) dilution, followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Low expression : confocal image showing no staining in mouse splenocytes (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Anti-mouse CD3 rat monoclonal antibody (Alexa Fluor® 647) was used to counterstain tubulin at 1/100 dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
Secondary antibody only control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution.
- WB
Lab
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : U-937.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (ab325932) at 1/1000 dilution
Lane 1:
BxPC-3 (human pancreas adenocarcinoma epithelial cell) whole cell lysate at 20 µg
Lane 2:
U-937 (human histiocytic lymphoma monocyte) 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 1/2000 dilution
Observed band size: 20 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (ab325932) at 1/1000 dilution
Lane 1:
Human stomach tissue lysate at 20 µg
Lane 2:
Human kidney 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 1/2000 dilution
Observed band size: 20 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Low expression : spleen, liver.
Samples are non-boiled as boiling may cause protein aggregation.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
Exposure time : Lanes 1-3 : 1 second, lanes 4-9 : 15 seconds
All lanes:
Western blot - Anti-Plasmolipin antibody [EPR31074-536] (ab325932) at 1/1000 dilution
Lane 1:
Human cerebellum tissue lysate at 20 µg
Lane 2:
Human sciatic nerve tissue lysate at 20 µg
Lane 3:
Human spleen tissue lysate at 20 µg
Lane 4:
Mouse stomach tissue lysate at 20 µg
Lane 5:
Mouse brain tissue lysate at 20 µg
Lane 6:
Mouse spleen tissue lysate at 20 µg
Lane 7:
Mouse liver tissue lysate at 20 µg
Lane 8:
Rat brain tissue lysate at 20 µg
Lane 9:
Rat spleen tissue lysate at 20 µg
Secondary
All lanes:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Observed band size: 20 kDa,36 kDa
false
- Dot
Lab
Dot Blot - Anti-Plasmolipin antibody [EPR31074-536] (AB325932)
Dot blot analysis of Plasmolipin using ab325932 at 1 : 1000 (0.5 µg/ml) followed by a Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1 : 100,000 dilution.
Lane 1 : Human Plasmolipin peptide
Lane 2 : Human Methylthioribose-1-phosphate isomerase peptide
Exposure time : 180 seconds.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
This antibody does not cross-react with human Methylthioribose-1-phosphate isomerase.
All lanes:
Dot Blot - Anti-Plasmolipin antibody [EPR31074-536] (ab325932) at 1/1000 dilution
Lane 1:
Human Plasmolipin peptide
Lane 2:
Human Methylthioribose-1-phosphate isomerase peptide
Secondary
All lanes:
Dot 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
false
Exposure time: 180s
Reactivity data
Product details
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.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
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