Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free
- BOND RX™ Validated
- Recombinant
- Advanced Validation
- RabMAb
- What is this?
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(3 Reviews)
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(1 Publication)
Rabbit Recombinant Monoclonal SOX10 antibody. Carrier free. Suitable for mIHC, IHC-Fr, IHC-P and reacts with Mouse, Rat, Human samples. Cited in 1 publication.
View Alternative Names
Transcription factor SOX-10, SOX10
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
This IHC data was generated using the same anti-SOX10 antibody clone, EPR4007-104, in a different buffer formulation (cat# ab180862).
Immunohistochemical analysis of paraffin-embedded Human fetal brain tissue labeling SOX10 with ab180862 at 1/100 dilution.
Heat mediated antigen retrieval was performed before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
This IHC data was generated using the same anti-SOX10 antibody clone, EPR4007-104, in a different buffer formulation (cat# ab180862).
Immunohistochemical analysis of paraffin-embedded Human melanoma tissue labeling SOX10 with ab180862 at 1/100 dilution.
Heat mediated antigen retrieval was performed before commencing with IHC staining protocol.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemical analysis of paraffin-embedded Human melanoma tissue labeling SOX10 with ab180862 at 1/100 dilution.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab180862).
Heat mediated antigen retrieval was performed before commencing with IHC staining protocol.
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemistry (Frozen) analysis of mouse cerebellum tissue sections labeling SOX10 with purified ab180862 at 1/50 (2.2 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/1000 (2 μg/ml) was used as the secondary antibody. Sections were fixed with 4% paraformaldehyde and permeabilised with 0.2% Triton X-100. Negative control : PBS instead of the primary antibody. DAPI (blue) was used as nuclear counterstain. Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20) was performed.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide ab180862).
- IHC-Fr
Lab
Immunohistochemistry (Frozen sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemistry (Frozen) analysis of rat cerebellum tissue sections labeling SOX10 with purified ab180862 at 1/50 (2.2 μg/ml). Goat anti rabbit IgG (Alexa Fluor® 488, ab150077) at 1/1000 (2 μg/ml) was used as the secondary antibody. Sections were fixed with 4% paraformaldehyde and permeabilised with 0.2% Triton X-100. Negative control : PBS instead of the primary antibody. DAPI (blue) was used as nuclear counterstain. Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20) was performed.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide ab180862).
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse cerebellum tissue sections labeling SOX10 with purified ab180862 at 1/500 (0.22 μg/ml). Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 minutes. Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) was used as the secondary antibody. Hematoxylin was used as a counterstain.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab180862).
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
This data was developed using ab180862, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse breast tissue staining Hormone sensitive lipase/HSL with ab325336 at a 1/2000 (0.248 μg/ml) dilution, ab324191 anti-E Cadherin used at a 1/500 (2.088 μg/ml) dilution and ab180862 anti-SOX10 used at a 1/4000 (0.03 μg/ml) dilution.
Panel A : anti-Hormone sensitive lipase/HSL (green; Opal™520), anti-E Cadherin (magenta; Opal™690), anti-SOX10 (gray; Opal™570) on mouse breast.
Panel B : anti-Hormone sensitive lipase/HSL staining adipocytes in mouse breast.
Panel C : anti-E Cadherin staining epithelium in mouse breast.
Panel D : anti-SOX10 staining on nucleus in mouse breast.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab325336, ab324191 and ab180862 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of Mouse cerebellum tissue labelling SOX1 with ab242125 at 1 : 2000 (0.29 ug/ml) dilution, RoR alpha/RORA with ab256799 at 1 : 800 (0.63 ug/ml) dilution and SOX10 with ab200078 at 1 : 5000 (0.2 ug/ml) followed by a ready to use secondary antibody Opal Polymer HRP Ms + Rb.
Panel A : merged staining of anti-SOX1 (magenta; Opal™690), anti-RORA (green; Opal™520) and anti-SOX10 (gray; Opal™570) on mouse cerebellum.
Panel B : anti-SOX1 staining Bergmann glia in mouse cerebellum.
Panel C : anti-RORA staining Pukinje cell and molecular layers in mouse cerebellum.
Panel D : anti-SOX10 staining glial cells in mouse cerebellum.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab242125, ab256799 and ab200078 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
- mIHC
Lab
Multiplex immunohistochemistry - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
This data was developed using ab180862, the same antibody clone in a different buffer formulation.
Multiplex immunohistochemistry analysis of formalin/PFA-fixed paraffin-embedded mouse breast tissue staining PNPLA3 with ab324436 at a 1/200 dilution, ab324191 anti-E Cadherin used at 1/500 dilution and ab180862 anti-SOX10 used at a 1/4000 dilution.
Panel A : anti-PNPLA3 (green; Opal™520), anti-E Cadherin (magenta; Opal™690) and anti-SOX10 (gray; Opal™570) on mouse breast.
Panel B : anti-PNPLA3 staining white adipose tissue in mouse breast.
Panel C : anti-E Cadherin staining membrane of epithelium in mouse breast.
Panel D : anti-SOX10 staining nucleus of epithelium in mouse breast.
Nuclear DNA was labeled with DAPI (shown in blue).
The section was incubated in three rounds of staining : in the order of ab324436, ab324191 and ab180862 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
- IHC-P
Unknown
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX10 antibody [EPR4007-104] - BSA and Azide free (AB220078)
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of mouse breast tissue sections labeling SOX10 with purified ab180862 at 1/500 (0.22 μg/ml). Antigen retrieval was heat mediated with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 20 minutes. Rabbit specific IHC polymer detection kit HRP/DAB (ab209101) was used as the secondary antibody. Hematoxylin was used as a counterstain.
This data was developed using the same antibody clone in a different buffer formulation containing PBS, BSA, glycerol, and sodium azide (ab180862).
Related conjugates and formulations (7)
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Anti-SOX10 antibody [EPR4007-104]
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603 Alexa Fluor® 568
Alexa Fluor® 568 Anti-SOX10 antibody [EPR4007-104]
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519 Alexa Fluor® 488
Alexa Fluor® 488 Anti-SOX10 antibody [EPR4007-104]
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665 Alexa Fluor® 647
Alexa Fluor® 647 Anti-SOX10 antibody [EPR4007-104]
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775 Alexa Fluor® 750
Alexa Fluor® 750 Anti-SOX10 antibody [EPR4007-104]
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617 Alexa Fluor® 594
Alexa Fluor® 594 Anti-SOX10 antibody [EPR4007-104]
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565 Alexa Fluor® 555
Alexa Fluor® 555 Anti-SOX10 antibody [EPR4007-104]
Reactivity data
Product details
ab220078 is the carrier-free version of ab180862.
Species reactivity
Mouse: We have preliminary internal testing data to indicate this antibody may not react with this species.
Please contact us for more information.
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.
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
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Storage information
Product protocols
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Target data
Publications (1)
Recent publications for all applications. Explore the full list and refine your search
Cell reports 43:114848 PubMed39392753
2024
Applications
Unspecified application
Species
Unspecified reactive species
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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