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>   首页   >   产品   >   一抗   >   精选抗体   >   磷酸化抗体   >   phospho-Sox2(S251) Antibody   

phospho-Sox2(S251) Antibody

Affinity Purified Rabbit Polyclonal Antibody (Pab)

     
  • 6 - phospho-Sox2(S251) Antibody AP3742a
    Dot blot analysis of anti-phospho-Sox2-pS251 Phospho-specific Pab (Cat. #AP3742a) on nitrocellulose membrane. 50ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.6ug per ml.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
DB, E
Primary Accession P48431
Other Accession P48432, NP_003097.1
Reactivity Human
Predicted Mouse
Host Rabbit
Clonality Polyclonal
Isotype Rabbit IgG
Additional Information
Other Names Transcription factor SOX-2, SOX2
Target/Specificity This Sox2 Antibody is generated from rabbits immunized with a KLH conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding S251 of human Sox2.
Dilution DB~~1:500
E~~Use at an assay dependent concentration.
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautionsphospho-Sox2(S251) Antibody is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

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).

REFERENCES

Gen, Y., et al. Cancer Genet. Cytogenet. 202(2):82-93(2010)
Ji, J., et al. Hum. Pathol. 41(10):1438-1447(2010)
Fang, X., et al. OMICS 14(4):369-384(2010)
Sholl, L.M., et al. Am. J. Surg. Pathol. 34(8):1193-1198(2010)
Zhang, D., et al. BMC Med. Genet. 11, 116 (2010) :

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