Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free
Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free
- RabMAb
- Recombinant
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Rabbit Recombinant Monoclonal SCG10 antibody. Carrier free. Suitable for I-ELISA, ICC/IF, IHC-P, WB and reacts with Recombinant full length protein - Mouse, Mouse, Human, Rat samples.
別名を表示する
Scg10, Scgn10, Stmb2, Stathmin-2, Superior cervical ganglion-10 protein, Protein SCG10, SCG10, SCGN10, STMN2, Stathmin-2, Superior cervical ganglion-10 protein, Protein SCG10, Scg10, Scgn10, Stathmin-2, Superior cervical ganglion-10 protein, Protein SCG10
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human Alzheimer's disease brain tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on human Alzheimer's disease brain. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human hippocampus tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on human hippocampus (PMID : 8622778). The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% TritonX-100 permeabilized SH-SY5Y (human neuroblastoma epithelial cell) and U-2 OS (human bone osteosarcoma epithelial cell) cells labelling with ab326937 at 1/2000 (0.252 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 SH-SY5Y cell line (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue).
Negative control : U-2 OS.
Image was taken with a confocal microscope (Leica-Microsystems TCS SP8).
ab7291 Anti-alpha Tubulin mouse monoclonal antibody was used to counterstain tubulin at 1/1000 (1 ug/ml) dilution followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1/1000 (2 ug/ml) dilution (Magenta).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Human kidney tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : no 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. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% TritonX-100 permeabilized mouse primary neural/glia cells labelling with ab326937 at 1/2000 (0.252 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 neural/glia cells (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). Confocal scanning Z step was set as 0.3 µm followed by image processing with maximum Z projection.
ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain at 1/500 dilution followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1 : 1000 dilution (Magenta).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% TritonX-100 permeabilized rat primary neural/glia cells labelling with ab326937 at 1/2000 (0.252 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 neural/glia cells (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). Confocal scanning Z step was set as 0.3 µm followed by image processing with maximum Z projection.
ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain at 1/500 dilution followed by ab150120 Goat Anti-Mouse IgG H&L (Alexa Fluor® 594) at 1 : 1000 dilution (Magenta).
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse Alzheimer's disease brain tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on mouse Alzheimer's disease brain. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat hippocampus tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on rat hippocampus. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat cerebrum tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on rat cerebrum. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse kidney tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : no staining on mouse kidney (PMID : 7812771). The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Rat kidney tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Low expression : no staining on rat kidney. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse hippocampus tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on mouse hippocampus. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded Mouse cerebrum tissue labeling with ab326937 at 1/500 (1.006 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive on mouse cerebrum. The primary antibody was incubated for 30 mins at room temperature.
The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Incubate slides with 3% Hydrogen Peroxide for 10 mins at room temperature after secondary antibody incubation to reduce the background.
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
- I-ELISA
Lab
Indirect ELISA - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Indirect ELISA analysis of ab326937 at 1000-0 ng/ml. The Secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1 : 2500 dilution dilution.
Antigen : Mouse Stathmin-1;Mouse Stathmin-2;Mouse Stathmin-3;Mouse Stathmin-4.
Antigen concentration : 1000 ng/ml
This antibody does not cross-react with mouse stathmin-1 stathmin-3 and stathmin-4 by ELISA.
- WB
Lab
Western blot - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : kidney spleen liver testis
Lanes 1-3 are incubated with Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 and lanes 4-9 are incubated with Goat Anti-Rabbit IgG (H+L) Peroxidase conjugated (ab97051) at 1/20000.
In Western blot Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] (<a href='/products/primary-antibodies/stathmin-2-stmn2-antibody-epr31028-544-ab326937'>ab326937</a>) at 1/1000 dilution
Lane 1:
Human cerebral cortex tissue lysate at 20 µg
Lane 2:
Human kidney tissue lysate at 20 µg
Lane 3:
Human spleen tissue lysate at 20 µg
Lane 4:
Mouse brain tissue lysate at 20 µg
Lane 5:
Mouse liver tissue lysate at 20 µg
Lane 6:
Mouse testis tissue lysate at 20 µg
Lane 7:
Rat brain tissue lysate at 20 µg
Lane 8:
Rat liver tissue lysate at 20 µg
Lane 9:
Rat testis tissue lysate at 20 µg
Secondary
Lanes 1 - 3:
Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Lanes 4 - 9:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 20 kDa,36 kDa
false
Exposure time: 180s
- WB
Lab
Western blot - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration : 5% NFDM/TBST.
Negative control : U-2 OS 293T NIH/3T3
In Western blot Anti-GAPDH antibody [EPR16891] - Loading Control (ab181602) (1 : 200000) (36KDa).
All lanes:
Western blot - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] (<a href='/products/primary-antibodies/stathmin-2-stmn2-antibody-epr31028-544-ab326937'>ab326937</a>) at 1/1000 dilution
Lane 1:
SK-N-BE(2) (human neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 2:
SK-N-SH (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3:
SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 4:
U-2 OS (human bone osteosarcoma epithelial cell) whole cell lysate at 20 µg
Lane 5:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 6:
Neuro-2a (mouse neuroblastoma neuroblast) whole cell lysate at 20 µg
Lane 7:
NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 8:
PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 20 kDa,36 kDa
false
Exposure time: 136s
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% TritonX-100 permeabilized mouse splenocyte cells labelling with ab326937 at 1/2000 (0.252 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Negative control : 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-rat CD3 mouse monoclonal antibody (Alexa Fluor® 647) was used to counterstain at 1/100 dilution (Magenta).
- ICC/IF
Lab
Immunocytochemistry/ Immunofluorescence - Anti-Stathmin-2/STMN2 antibody [EPR31028-544] - BSA and Azide free (AB328102)
This data was developed using ab326937, the same antibody clone in a different buffer formulation.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed 0.1% TritonX-100 permeabilized rat splenocyte cells labelling with ab326937 at 1/2000 (0.252 µg/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 dilution (Green).
Negative control : 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-human CD3 mouse monoclonal antibody (Alexa Fluor® 647) was used to counterstain at 1/100 dilution (Magenta).
関連する標識済み抗体及び組成の異なる製品 (1)
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Anti-Stathmin-2/STMN2 antibody [EPR31028-544]
Reactivity data
製品の詳細
ab328102 is the carrier-free version of ab326937.
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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