ARG66767
anti-SOX2 antibody [SQab20200]
anti-SOX2 antibody [SQab20200] for IHC-Formalin-fixed paraffin-embedded sections and Human
Overview
Product Description | Recombinant Rabbit Monoclonal antibody [SQab20200] recognizes SOX2 |
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Tested Reactivity | Hu |
Tested Application | IHC-P |
Host | Rabbit |
Clonality | Monoclonal |
Clone | SQab20200 |
Isotype | IgG |
Target Name | SOX2 |
Antigen Species | Human |
Immunogen | Synthetic peptide within aa. 1-100 of Human SOX2. |
Conjugation | Un-conjugated |
Alternate Names | Transcription factor SOX-2; MCOPS3; ANOP3 |
Application Instructions
Application Suggestion |
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Application Note | IHC-P: Antigen Retrieval: Heat mediation was performed in Tris/EDTA buffer (pH 9.0). * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. |
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Positive Control | Lung squamous cell carcinomas tissue. |
Properties
Form | Liquid |
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Purification | Purification with Protein A. |
Buffer | PBS, 0.01% Sodium azide, 40% Glycerol and 0.05% BSA. |
Preservative | 0.01% Sodium azide |
Stabilizer | 40% Glycerol and 0.05% BSA |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links | |
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Gene Symbol | SOX2 |
Gene Full Name | SRY (sex determining region Y)-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] |
Function | 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 (By similarity). 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 (By similarity). Keeps neural cells undifferentiated by counteracting the activity of proneural proteins and suppresses neuronal differentiation (By similarity). [UniProt] |
Cellular Localization | Nucleus. [UniProt] |
Calculated MW | 34 kDa |
PTM | Sumoylation inhibits binding on DNA and negatively regulates the FGF4 transactivation. [UniProt] |