TFII-I (phospho Tyr248) rabbit pAb

TFII-I (phospho Tyr248) rabbit pAb

AO-06-ES5689-100

TFII-I (phospho Tyr248) rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES5689
Product nameTFII-I (phospho Tyr248) rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameGTF2I; BAP135; WBSCR6; General transcription factor II-I; GTFII-I; TFII-I; Bruton tyrosine kinase-associated protein 135; BAP-135; BTK-associated protein 135; SRF-Phox1-interacting protein; SPIN; Williams-Beuren syndrome chromosomal region
Size100μL
Unit price ($)248
Human gene ID2969
Human Swiss-ProtP78347
SourceRabbit
IsotypeIgG
TargetTFII-I
Fields>>Basal transcription factors;>>cGMP-PKG signaling pathway
Gene nameGTF2I
Protein nameGeneral transcription factor II-I
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID14886
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9ESZ8
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID353256
Rat gene linkView Rat Gene
Rat Swiss-ProtQ5U2Y1
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human TFII-I around the phosphorylation site of Tyr248. AA range:214-263
SpecificityPhospho-TFII-I (Y248) Polyclonal Antibody detects endogenous levels of TFII-I protein only when phosphorylated at Y248.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)115kD
Backgroundgeneral transcription factor IIi(GTF2I) Homo sapiens This gene encodes a phosphoprotein containing six characteristic repeat motifs. The encoded protein binds to the initiator element (Inr) and E-box element in promoters and functions as a regulator of transcription. This locus, along with several other neighboring genes, is deleted in Williams-Beuren syndrome. There are many closely related genes and pseudogenes for this gene on chromosome 7. This gene also has pseudogenes on chromosomes 9, 13, and 21. Alternatively spliced transcript variants encoding multiple isoforms have been observed. [provided by RefSeq, Jul 2013],
Functiondisease:Haploinsufficiency of GTF2I may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS), a rare developmental disorder. It is a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23.,function:Interacts with the basal transcription machinery by coordinating the formation of a multiprotein complex at the C-FOS promoter, and linking specific signal responsive activator complexes. Promotes the formation of stable high-order complexes of SRF and PHOX1 and interacts cooperatively with PHOX1 to promote serum-inducible transcription of a reporter gene deriven by the C-FOS serum response element (SRE). Acts as a coregulator for USF1 by binding independently two promoter elements, a pyrimidine-rich initiator (Inr) and an upstream E-box. Required for the formation of functional ARID3A DNA-binding complexes
Subcellular locationCytoplasm . Nucleus . Colocalizes with BTK in the cytoplasm.
ExpressionUbiquitous. Isoform 1 is strongly expressed in fetal brain, weakly in adult brain, muscle, and lymphoblasts and is almost undetectable in other adult tissues, while the other isoforms are equally expressed in all adult tissues.

Additional Images

Image 1
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Enzyme-Linked Immunosorbent Assay (Phospho-ELISA) for Immunogen Phosphopeptide (Phospho-left) and Non-Phosphopeptide (Phospho-right), using TFII-I (Phospho-Tyr248) Antibody
Image 2
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Western blot analysis of lysates from LOVO cells, using TFII-I (Phospho-Tyr248) Antibody. The lane on the right is blocked with the phospho peptide.
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: AO-06-ES5689-100
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