Comparison

SOX2 Antibody

Manufacturer ProSci
Category
Type Antibody Polyclonal
Specific against Human, Mouse, Rat
Format Liquid
Applications WB, ELISA
Amount 100 ul
Host Rabbit
Item no. PRS-31-255-100ul
eClass 6.1 32160702
eClass 9.0 32160702
Available
Shipping
blue ice or RT
By Research Area
Transcription
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human SOX2.
Applications
SOX2 antibody can be used for detection of SOX2 by ELISA at 1:12500. SOX2 antibody can be used for detection of SOX2 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.
Positive Control 1
OVCAR-3 Cell Lysate
Predicted Molecular Weight
34 kDa
Purification
Antibody is purified by peptide affinity chromatography method.
Clonality
Polyclonal
Conjugate
Unconjugated
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration
batch dependent
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store SOX2 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Disclaimer
This product is for research use only.
Modifications
None
Ncbi Official Symbol
SOX2
Accession #
NP_003097
Protein Gi #
28195386
Ncbi Gene Id #
6657
User Note
Optimal dilutions for each application to be determined by the researcher.
Ncbi Official Symbol
SOX2
Ncbi Official Full Name
SRY (sex determining region Y)-box 2
Ncbi Organism
Homo sapiens
Swissprot #
P48431
Background
SOX2 is a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in this gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation. This intronless gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of this gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. Mutations in this gene have been associated with optic nerve hypoplasia and with syndromic microphthalmia, a severe form of structural eye malformation. This gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Background References 1
Wang, P., (2008) Arch. Ophthalmol. 126 (5), 709-713 .
1st Image Caption
Antibody used in IHC.
2nd Image Caption
Antibody used in WB on Human OVCAR-3 at 0.2-1 ug/ml.
3rd Image Caption
Antibody used in IHC on Human Spleen.
4th Image Caption
Antibody used in IHC on Human Kidney.
5th Image Caption
Antibody used in WB on U87 at 1:1000.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ul
Available: In stock
available

Delivery expected until 7/4/2024 

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