- Datasheet
- Specific References (191)
- Protocols
Overview
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Product nameAnti-SOX2 antibody
See all SOX2 primary antibodies -
DescriptionRabbit polyclonal to SOX2
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Host speciesRabbit
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Tested applicationsSuitable for: IHC-P, ICC/IF, IP, WB, IHC - Wholemount, IHC-Frmore details
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Species reactivityReacts with: Mouse, Rat, Horse, Chicken, Human, Pig, Xenopus laevis, Zebrafish, Quail, Rainbow trout, Spotted catshark, Thornback ray
Predicted to work with: Sheep, Cow, Rhesus monkey
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Immunogen
Synthetic peptide conjugated to KLH derived from within residues 300 to the C-terminus of Human SOX2.
(Peptide available as ab97974.)
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Positive control
- This antibody gave a positive signal in NCCIT, F9 and C6 Whole Cell Lysates.
Properties
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FormLiquid
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Storage instructionsShipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
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Storage bufferpH: 7.40
Preservative: 0.02% Sodium azide
Constituent: PBS
Note: Batches of this product that have a concentration < 1mg/ml may have BSA added as a stabilising agent. If you would like information about the formulation of a specific lot, please contact our scientific support team who will be happy to help. -
Concentration information loading... -
PurityImmunogen affinity purified
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ClonalityPolyclonal
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IsotypeIgG
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Research areas
Associated products
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Alternative Versions
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Compatible Secondaries
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Positive Controls
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Applications
Our Abpromise guarantee covers the use of ab97959 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| Application | Abreviews | Notes |
|---|---|---|
| IHC-P | 1/1000 - 1/2000. | |
| ICC/IF | Use a concentration of 1 µg/ml. We recommend Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody. |
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| IP | Use at an assay dependent concentration. | |
| WB | Use a concentration of 1 µg/ml. Detects a band of approximately 34,40 kDa (predicted molecular weight: 34 kDa). | |
| IHC - Wholemount | 1/200. | |
| IHC-Fr | Use at an assay dependent concentration. |
Target
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FunctionTranscription factor that forms a trimeric complex with OCT4 on DNA and controls the expression of a number of genes involved in embryonic development such as YES1, FGF4, UTF1 and ZFP206 (By similarity). Critical for early embryogenesis and for embryonic stem cell pluripotency.
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Involvement in diseaseDefects in SOX2 are the cause of microphthalmia syndromic type 3 (MCOPS3) [MIM:206900]. Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS3 is characterized by the rare association of malformations including uni- or bilateral anophthalmia or microphthalmia, and esophageal atresia with trachoesophageal fistula.
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Sequence similaritiesContains 1 HMG box DNA-binding domain.
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Post-translational
modificationsSumoylation inhibits binding on DNA and negatively regulates the FGF4 transactivation. -
Cellular localizationNucleus.
- Information by UniProt
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Database links
- Entrez Gene: 396105 Chicken
- Entrez Gene: 784383 Cow
- Entrez Gene: 6657 Human
- Entrez Gene: 20674 Mouse
- Entrez Gene: 407739 Pig
- Entrez Gene: 499593 Rat
- Entrez Gene: 398000 Xenopus laevis
- Entrez Gene: 378723 Zebrafish
see all -
Alternative names
- ANOP3 antibody
- cb236 antibody
- Delta EF2a antibody
see all
Images
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Immunocytochemistry/ Immunofluorescence - Anti-SOX2 antibody (ab97959)Cell line: NCCIT (human pluripotent embryonal carcinoma)
Target AbID: Ab97959 anti-Sox2, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody was used.
Counterstain AbID: Ab7291 anti-Tubulin (Rabbit mAb), 97959
Fixative: 4% PFA
Permeabilisation: 0.1% Triton-X
Nuclear counter stain: DAPI
Comments: Confocal image showing negative staining on NCCIT cells
Target primary antibody dilution: 1:500
Target secondary antibody dilution: 1:1000 (2ug/mL)
Counterstain primary antibody dilution: 1:1000 (1ug/mL)
Counterstain secondary antibody dilution: 1:1000 (2ug/mL)
Negative control 1 primary antibody dilution: 1:500 (Ab97959)
Negative control 1 secondary antibody dilution: 1:1000 (2ug/mL) (Ab150120)
Negative control 2 primary antibody dilution: 1:1000 (1ug/mL) (Ab7291)
Negative control 2 secondary antibody dilution: 1:1000 (2ug/mL) (Ab150077)
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Immunocytochemistry/ Immunofluorescence - Anti-SOX2 antibody (ab97959)ICC/IF image of ab97959 stained mouse embryonic stem cells. The cells were 4% formaldehyde fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab97959, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM. -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United KingdomIHC-P image of SOX2 (ab97959) on E13 mouse Spinal Cord sections. The sections were fixed in formaldehyde and underwent heat mediated Anigen retrieval using citric acis (pH6). The sections were then blocked in 1% BSA solution for 10 mins at 21°C. -
Western blot - Anti-SOX2 antibody (ab97959)All lanes : Anti-SOX2 antibody (ab97959) at 1 µg
Lane 1 : NCCIT (Human embryonic carcinoma cell line) Whole Cell Lysate
Lane 2 : F9 (Mouse embryonic carcinoma cell line) Whole Cell Lysate
Lane 3 : MCF7 (Human breast adenocarcinoma cell line) Whole Cell Lysate
Lane 4 : C6 (Rat glioma cell line) Whole Cell Lysate
Lane 5 : Hippocampus (Rat) Tissue Lysate
Lane 6 : Spinal Cord (Rat) Tissue Lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Blots were developed with goat anti-rabbit IgG (H+L) and goat anti-mouse IgG (H+L) secondary antibodies at 1/10,000 dilution for 1 h at room temperature before imaging.
Performed under reducing conditions.
Predicted band size: 34 kDa
Observed band size: 40 kDa (why is the actual band size different from the predicted?)Green signal from target - ab97959 observed at 40 kDa
Red signal from loading control ab9484 (GAPDH) observed at 37 kDa -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United KingdomIHC-P image of SOX2 (ab97959) on zebrafish developing retina sections. The sections were fixed in formaldehyde and underwent heat mediated Anigen retrieval using citric acis (pH6). The sections were then blocked in 1% BSA solution for 10 mins at 21°C. The upper section used Abcam's EXPOSE HRP-DAB polyvalent kit (ab80436). The lower section was immunostained using my std stABCpx-DAB method. -
Western blot - Anti-SOX2 antibody (ab97959)All lanes : Anti-SOX2 antibody (ab97959) at 1 µg/ml
Lane 1 : IOUD2 (Mouse embryonic stem cell) Whole Cell Lysate
Lane 2 : HUES7 (Human embryonic stem cell line) Whole Cell Lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 34 kDa
Observed band size: 43 kDa (why is the actual band size different from the predicted?)
Additional bands at: 37 kDa, 39 kDa. We are unsure as to the identity of these extra bands.
Exposure time: 3 minutes -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United KingdomIHC-P image of SOX2 (ab97959) on E7 Chicken brain sections. The sections were fixed in formaldehyde and underwent heat mediated Anigen retrieval using citric acis (pH6). The sections were then blocked in 1% BSA solution for 10 mins at 21°C. The upper section used Abcam's EXPOSE HRP-DAB polyvalent kit (ab80436). The lower section was immunostained using my std stABCpx-DAB method. -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United KingdomIHC-P image of SOX2 (ab97959) on Adult rat brain sections. The sections were fixed in formaldehyde and underwent heat mediated Anigen retrieval using citric acis (pH6). The sections were then blocked in 1% BSA solution for 10 mins at 21°C. Upper image using EXPOSE HRP-DAB polyvalent kit (ab80436) shows strong, clear immunostaining of many nuclei in the subventricular region of the lateral ventricle ( double-red arrowhead) and also of the ependymal cells lining the ventricle ( black arrowheads). Direction of migration indicated by green arrows. -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an abreview submitted by Carl Hobbs, King's College London, United KingdomIHC-P image of SOX2 (ab97959) on E9 Quail developing retina sections. The sections were fixed in formaldehyde and underwent heat mediated Anigen retrieval using citric acis (pH6). The sections were then blocked in 1% BSA solution for 10 mins at 21°C. -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SOX2 antibody (ab97959)This image is courtesy of an anonymous Abreviewab97959 staining SOX2 in Spotted Catshark (Scyliorhinus canicula) eye tissue sections by Immunohistochemistry (IHC-P - paraformaldehyde-fixed, paraffin-embedded sections).
Tissue was fixed with paraformaldehyde and antigen retrieval was by heat mediation in citrate buffer. Samples were incubated with primary antibody (1/500 in TBS + 1% BSA) for 12 hours at 4°C. An HRP-conjugated goat anti-rabbit polyclonal IgG (1/200) was used as the secondary antibody. -
IHC - Wholemount - Anti-SOX2 antibody (ab97959)This image is courtesy of an anonymous abreview.IHC-Wholemount image of anti-Sox2 antibody (ab97959) staining on a mouse embryo. This embryo was stained with anti-Sox2 antibody (green) for 48 hours at 4°C. Nuclei stained with DAPI (grey). -
IHC - Wholemount - Anti-SOX2 antibody (ab97959)This image is courtesy of an anonymous AbreviewIHC - Wholemount of Xenopus laevis embryo labelling SOX2 with ab697959. Sample was incubated with primary antibody (1/250) for 12 hours at 4°C. An Alkaline Phosphatase-conjugated mouse anti-rabbit IgG monoclonal (1/1000) was used as the secondary antibody.
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Immunocytochemistry/ Immunofluorescence - Anti-SOX2 antibody (ab97959)Cell line: NIH/3T3 (mouse embryonic fibroblast cell line)
Target AbID: Ab97959 anti-Sox2, used Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077) secondary antibody
Counterstain AbID: Ab7291 anti-Tubulin (Rabbit mAb), Ab150120 AlexaFluor®594 Goat anti-Mouse secondary
Fixative: 4% PFA
Permeabilisation: 0.1% Triton-X
Nuclear counter stain: DAPI
Comments: Confocal image showing negative staining on NIH/3T3 cells
Target primary antibody dilution: 1:500
Target secondary antibody dilution: 1:1000 (2ug/mL)
Counterstain primary antibody dilution: 1:1000 (1ug/mL)
Counterstain secondary antibody dilution: 1:1000 (2ug/mL)
Negative control 1 primary antibody dilution: 1:500 (Ab97959)
Negative control 1 secondary antibody dilution: 1:1000 (2ug/mL) (Ab150120)
Negative control 2 primary antibody dilution: 1:1000 (1ug/mL) (Ab7291)
Negative control 2 secondary antibody dilution: 1:1000 (2ug/mL) (Ab150077)
Protocols
References
This product has been referenced in:
- Yoshimura A et al. TheSox2promoter-driven CD63-GFP transgenic rat model allows tracking of neural stem cell-derived extracellular vesicles. Dis Model Mech 11:N/A (2018). WB, ICC/IF ; Rat . Read more (PubMed: 29208635) »
- Weeratunga P et al. Induced Pluripotent Stem Cells from a Marsupial, the Tasmanian Devil (Sarcophilus harrisii): Insight into the Evolution of Mammalian Pluripotency. Stem Cells Dev 27:112-122 (2018). ICC/IF . Read more (PubMed: 29161957) »
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