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GTF2I Peptide - middle region (AAP58007)

ArtNr AAP58007
Hersteller AVIVA Systems Biology
Menge 100 ug
Kategorie
Typ Peptides
Format Lyophilized powder
Applikationen WB
Specific against other
ECLASS 10.1 32160409
ECLASS 11.0 32160409
UNSPSC 12352202
Alias BAP-135, BAP135, BTKAP1, DIWS, IB291, SPIN, TFII-I, WBS, WBSCR6
Similar products GTF2I
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Description
This is a synthetic peptide designed for use in combination with anti-GTF2I antibody (Catalog #: ARP58007_P050) made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Gene symbol
GTF2I
Protein size
998
Molecular weight
112kDa
Product format
Lyophilized powder
Gene id
2969
Reconstitution and storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Partner proteins
ATF6, BTK, GTF2I, HDAC3, JAK2, MAPK3, MYC, NFKB2, PIAS2, PRKG1, PRRX1, SMAD2, SRC, SRF, STAT1, STAT3, USF1, YY1, ZBTB17, ATF6, BTK, HDAC1, HDAC2, HDAC3, HDAC3, KDM1A, MAPK3, MEPCE, MYC, NAA38, NFI1, OTUB2, PHF21A, PRKG1, PRRX1, PTP4A3, Pias2, SRF, STAT1, STAT3, STX7, SUZ12, USF1, USP7
Description of target
GTF2I is a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon(s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants. This gene encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. Four transcript variants encoding different isoforms have been found for this gene.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 100 ug
Lieferbar: In stock
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