Sox2 antibody (pAb)
Host / Isotype
Rabbit / IgG
Reactivity
Human, Mouse
Applications
ChIP, ChIP-Seq, ICC, IF, WB
Cat No : 39843,39844 39843
Synonyms
验证数据展示
产品信息
Tested Applications |
ChIP, ChIP-Seq, ICC, IF, WB
Applications Validated by Active Motif: ChIP: 10 ul per ChIP ChIP-Seq: 10 ul each ICC/IF: 1:200 dilution WB: 1:500 - 1:1,000 dilution ChIP-Seq validation was performed by Active Motif's Epigenetics Services; the complete data set is available in the UCSC Genome Browser by clicking here. |
Tested Reactivity | Human, Mouse |
Host / Isotype | Rabbit / IgG |
Class | Polyclonal |
Type | Antibody |
Immunogen | This Sox2 antibody was raised against a peptide within the C-terminal region of human Sox2. |
Full Name | Sox2 antibody (pAb) |
Synonyms | Sox2, SRY related HMG BOX gene 2, sox, sox 2, sox-2, embryogenesis, embryonic stem cell pluripotency, es cell, esc, Induced Pluripotency, microphthalmia, sample |
Molecular weight | 42 kDa |
GenBank accession number | NP_003097 | RRID | AB_2750954 | Purification Method | Affinity Purified |
Buffer | Purified IgG in 70 mM Tris (pH 8), 105 mM NaCl, 31 mM glycine, 0.07 mM EDTA, 30% glycerol and 0.035% sodium azide. Sodium azide is highly toxic. |
Storage | Some products may be shipped at room temperature. This will not affect their stability or performance. Avoid repeated freeze/thaw cycles by aliquoting items into single-use fractions for storage at -20°C for up to 2 years. Keep all reagents on ice when not in storage. |
背景介绍
Sox2 (SRY related HMG BOX gene 2) is a DNA binding transcription factor and a member of the SOX family of proteins. SOX proteins have an HMG box that binds DNA. Sox2 forms a complex with Oct-4 and controls the expression of a number of genes involved in embryonic. Sox2 is critical for early embryogenesis and for embryonic stem cell pluripotency and thus can serve as a stem cell marker. Overexpression of Sox2 (along with Oct-4, KLF4 and c-Myc) can transform mouse fibroblasts into a state resembling embryonic stem cells (ES cells), referred to as Induced Pluripotency. Defects in Sox2 are the cause of microphthalmia syndromic type 3.