SOX2 polyclonal antibody
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More Files
- More Functions
Western Blot (Cell lysate)
Western blot analysis of BALB/3T3 cells with SOX2 polyclonal antibody (Cat # PAB19185) at (Lane 1) 1 and (Lane 2) 2 ug/mL dilution.
Immunocytochemistry
Immunocytochemical staining of BALB/3T3 cells with SOX2 polyclonal antibody (Cat # PAB19185) at 5 ug/mL dilution.
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Specification
Product Description
Rabbit polyclonal antibody rasied against synthetic peptide of SOX2.
Immunogen
A synthetic peptide corresponding to 15 amino acids near N-terminus of human SOX2.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Form
Liquid
Purification
Peptide affinity purification
Concentration
1 mg/mL
Recommend Usage
Western Blot (1-2 ug/mL)
Immunocytochemistry (5 ug/mL)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.02% sodium azide)
Storage Instruction
Store at 4°C for three months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Cell lysate)
Western blot analysis of BALB/3T3 cells with SOX2 polyclonal antibody (Cat # PAB19185) at (Lane 1) 1 and (Lane 2) 2 ug/mL dilution.Immunocytochemistry
Immunocytochemical staining of BALB/3T3 cells with SOX2 polyclonal antibody (Cat # PAB19185) at 5 ug/mL dilution.Enzyme-linked Immunoabsorbent Assay
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Gene Info — SOX2
Entrez GeneID
6657Protein Accession#
NP_003097Gene Name
SOX2
Gene Alias
ANOP3, MCOPS3, MGC2413
Gene Description
SRY (sex determining region Y)-box 2
Gene Ontology
HyperlinkGene Summary
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). [provided by RefSeq
Other Designations
SRY-related HMG-box gene 2|sex-determining region Y-box 2|transcription factor SOX2
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Interactome
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Disease
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