Vergleich

SOX2 (SRY (sex determining region Y)-box 2)

ArtNr 18-003-44073
Hersteller GENWAY
Menge 0.1 mg
Kategorie
Typ Antibody
Applikationen WB
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-CF53BE
Similar products 18-003-44073
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Genway ID:
GWB-CF53BE
Antigen Specificity:
Polyclonal antibody produced in rabbits immunized with a synthetic peptide corresponding to a region of Human SOX2.
ELISA Titre:
1:1562500
Category:
Transcription Factor Antibodies
Note:
Suggested starting concentrations are provided. Optimal dilutions should be determined by end-user. Differences in calculated versus apparent molecular weight may be due to post-translational modifications or protein hydrophobicity. 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
Function:
Can form ternary complexes with OCT-1 or OCT-3 but acts as a transcriptional activator of FGF-4 enhancer DNA sequences only in conjunction with OCT-3 (By similarity).
Subcellular Location:
Nucleus.
Disease:
Defects in SOX2 are the cause of microphthalmia syndromic type 3 (MCOPS3) [MIM:206900]. MCOPS3 is characterized by the association of microphthalmia or clinical anophthalmia with anomalies such as microcephaly short stature hypogonadotropic hypogonadism esophageal atresia and neurologic manifestations.
Similarity:
Contains 1 HMG box DNA-binding domain. 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 protein lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). Lei. J. X. . (2005) Cell Death Differ. 12 (11). 1368-1377.

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Menge: 0.1 mg
Lieferbar: In stock
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