Comparison

GTF2I Peptide - middle region (AAP58007)

Item no. AAP58007
Manufacturer AVIVA Systems Biology
Amount 100 ug
Category
Type Peptides
Format Lyophilized powder
Applications 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
Available
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.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 100 ug
Available: In stock
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