KO Validated Antibodies 2
Anti-SOX2 Antibody [KO Validated] (CAB19118)
- SKU:
- CAB19118
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Description
Antibody Name: | Anti-SOX2 Antibody [KO Validated] |
Antibody SKU: | CAB19118 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | A synthesized peptide derived from human SOX2 |
Application: | WB |
Recommended Dilution: | WB 1:500 - 1:2000 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | Mouse brain, Rat brain, 293T |
Immunogen: | A synthesized peptide derived from human SOX2 |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 0.05% BSA, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 6657 |
Uniprot: | P48431 |
Cellular Location: | |
Calculated MW: | 34kDa |
Observed MW: | 38kDa |
Synonyms: | ANOP3, MCOPS3, SOX2, SRY-box 2 |
Background: | 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, Jul 2008] |
UniProt Protein Function: | SOX2: Transcription 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. Critical for early embryogenesis and for embryonic stem cell pluripotency. May function as a switch in neuronal development. Downstream SRRT target that mediates the promotion of neural stem cell self-renewal. Keeps neural cells undifferentiated by counteracting the activity of proneural proteins and suppresses neuronal differentiation. Interacts with ZSCAN10. Interacts with SOX3 and FGFR1. |
UniProt Protein Details: | Protein type:Cell development/differentiation; DNA-binding; Transcription factor Chromosomal Location of Human Ortholog: 3q26.33 Cellular Component: cytoplasm; cytosol; nucleoplasm; nucleus; transcription factor complex Molecular Function:DNA binding; miRNA binding; protein binding; sequence-specific DNA binding; transcription factor activity Biological Process: cell cycle arrest; endodermal cell fate specification; eye development; forebrain development; inner ear development; negative regulation of epithelial cell proliferation; negative regulation of neuron differentiation; negative regulation of transcription from RNA polymerase II promoter; osteoblast differentiation; pituitary gland development; positive regulation of MAPKKK cascade; positive regulation of transcription from RNA polymerase II promoter; positive regulation of transcription, DNA-dependent; regulation of caspase activity; regulation of gene expression; regulation of transcription, DNA-dependent; response to wounding; somatic stem cell maintenance Disease: Microphthalmia, Syndromic 3; Tracheoesophageal Fistula With Or Without Esophageal Atresia |
NCBI 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, Jul 2008] |
UniProt Code: | P48431 |
NCBI GenInfo Identifier: | 1351091 |
NCBI Gene ID: | 6657 |
NCBI Accession: | P48431.1 |
UniProt Secondary Accession: | P48431,Q14537, |
UniProt Related Accession: | P48431 |
Molecular Weight: | 34kDa |
NCBI Full Name: | Transcription factor SOX-2 |
NCBI Synonym Full Names: | SRY-box 2 |
NCBI Official Symbol: | SOX2 |
NCBI Official Synonym Symbols: | ANOP3; MCOPS3 |
NCBI Protein Information: | transcription factor SOX-2 |
UniProt Protein Name: | Transcription factor SOX-2 |
UniProt Gene Name: | SOX2 |