Basic infomation |
source |
Mouse |
Clonality |
Polyclonal |
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Isotype |
IgG |
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Reactivity |
H M R |
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MW (kDa) |
34kDa |
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Purification |
Antigen affinity purfication |
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UniProt ID |
P48431 |
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NCBI Gene |
6657 |
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Applications |
Tested Applications |
WB, |
Cited Applications |
WB, IHC, IF |
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Product Usage Information |
Western Blotting |
1:1000-1:2000 |
Immunohistochemistry |
1:200-1:400 |
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Immunofluorescence |
1:200-1:400 |
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Storage |
PBS with 50% glycerol and less than 0.02% sodium azide |
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Store at –20°C, stable for one year after shipment |
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Do not aliquot the antibody |
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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). |
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Abbreviation |
H: human M: mouse R: rat Rb: rabbit Hm: hamster Mk: monkey Vir: virus C: chicken Z: zebrafish Dg: dog Pg: pig Hr: horse |