SOX10 Rabbit Monoclonal Antibody(ARA758)
WB | 1:1000-1:2000 |
IHC | 1:1000-1:2000 |
IF/ICC | 1:20-1:50 |
FC | 1:200-1:1000 |
IP | 1:502 |
Description | Rabbit Monoclonal Antibody to SOX10 |
Antibody Type | Primary antibody |
Predicted MW | 50kDa |
Immunogen | A synthetic peptide corresponding to SOX10 residues within aa400-500 of SOX10 was used as an immunogen. |
Purification | ProA affinity purified IgG |
Form/Buffer | PBS 59%, Sodium azide 0.01%, Glycerol 40%, BSA 0.33%. |
Alternative Names | Transcription factor SOX-10 |
Gene Symbol | SOX10 |
Entrez Gene | 6663(Human) |
Swissprot | P56693 |
*Clone Number, Reactivity, Source/Host and Clonality can be found in the product name and Key Features section above.

All lane: Anti-SOX10 antibody at 1:1,000 dilution
Predicted MW: 50 kDa
Observed MW: 58 kDa
Lane 1: A375
Lysate at 10 µg per lane
2nd Ab:
G&R HRP(H+L) 1:10,000
Exposure: 120s

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human melanoma tissue labelling SOX10 with ARA758 at 1:1,600. Heat mediated antigen retrieval was performed using Tris/EDTA buffer pH 9.0.

SOX10 was immunoprecipitated from 0.4mg of A375 lysate with ARA758 at 1:50 dilution.
2nd Ab:
GAR HRP for IP 1:500
Lane 1: ARA758 IP in A375 whole cell lysate
Lane 2: Rabbit IgG instead of ARA758 in A375 whole cell lysate
Lane3: A375 whole cell lysate, 10 µg(input)
Exposure: 120s

Overlay histogram showing A375 cells stained with ARA758 (blue). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% TritonX-100 for 15 min. The cells were then incubated in the antibody (ARA758, 1:1,000 dilution) in 1x PBS/1% BSA for 30 min at room temperature. The secondary antibody used was a Goat Anti-Rabbit Alexa Fluor<sup>®</sup> 488 (IgG H+L) at 1:2,000 dilution for 20 min at room temperature. Unlabelled sample (red) was used as a control.

ARA758 staining SOX10 in A375 cells by IF/ICC (immunofluorescence/immunocytochemistry). Cells were fixed with paraformaldehyde, permeabilized with 0.1% Triton X-100 and blocked with 10% goat serum for half an hour at room temperature. Samples were incubated with primary antibody (1:10,000) at 4°C. An Alexa Fluor<sup>®</sup> 488-conjugated Goat Anti-Rabbit IgG polyclonal was used as the secondary antibody (1:500). DAPI (blue) was used as the nuclear counter stain.
Control: PBS and secondary antibody, An Alexa Fluor<sup>®</sup> 488-conjugated Goat Anti-Rabbit IgG (1:500).
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