Catalog Number:
CPTC-ZEB2-1
Target Antigen:
Zinc Finger E-Box Binding Homeobox 2 Peptide 1
Isotype:
IgG
Species:
Rabbit Monoclonal Antibody
Last Updated:
02/09/2024
Antigen Recognition(s):
Peptide, Recombinant Full-length, Endogenous
Thematic Panel(s):
Epithelial Mesenchymal Transition (EMT)
Result: Negative
This PDF contains the evaluation results provided by the Human Protein Atlas (www.proteinatlas.org)
Result: Negative
Immuno-precipitation data obtained incubating CPTC-ZEB2-1 and the recombinant domain of ZEB2 (aa647-1214, expected, MW ~64KDa)
Result: Positive
Western Blot using CPTC-ZEB2-1 as primary antibody against recombinant ZEB2 protein domain comprising amino acids 647-1214 (lane 2) with expected MW of 58.1 KDa. Molecular weight standards are also included (lane 1).
Result: Positive
Western Blot using CPTC-ZEB2-1 as primary antibody against cell lysates A549, H226, HeLa, Jurkat and MCF7. Expected MW of 136 KDa. Positive for A549, Hela, Jurkat and weak for H226 and MCF7. Molecular weight standards are also included (lane 1).
Result: Negative
Automated Western Blot using CPTC-ZEB2-1 as primary antibody against cell lysates A549, H226, HeLa, Jurkat and MCF7. Expected MW of 136 KDa. All cell lysates negative. Molecular weight standards are also included (lane 1).
NCI Identification Number:
00074
Antigen Name:
Zinc Finger E-Box Binding Homeobox 2 Peptide 1
CPTC Name:
CPTC-ZEB2 Peptide 1
Aliases:
Zinc Finger E-Box Binding Homeobox 2; ZFHX1B; SIP1; SMADIP1; Zinc Finger Homeobox 1b; SMAD Interacting Protein 1; HSPC082; SIP-1; KIAA0569; ZFX1B; Zinc Finger Homeobox Protein 1b
Function:
This gene encodes a zinc finger transcription factor. The encoded protein likely plays a role in transcriptional repression of interleukin 2. Mutations in this gene have been associated with posterior polymorphous corneal dystrophy-3 and late-onset Fuchs endothelial corneal dystrophy. Alternatively spliced transcript variants encoding different isoforms have been described.
ZEB1 (zinc finger E-box binding homeobox 1) is a protein-coding gene. Diseases associated with ZEB1 include corneal dystrophy, posterior polymorphous, 3, and corneal dystrophy, fuchs endothelial, 6. GO annotations related to this gene include transcription coactivator activity and sequence-specific DNA binding transcription factor activity. An important paralog of this gene is ZEB2.
Acts as a transcriptional repressor. Inhibits interleukin-2 (IL-2) gene expression. Enhances or represses the promoter activity of the ATP1A1 gene depending on the quantity of cDNA and on the cell type. Represses E-cadherin promoter and induces an epithelial-mesenchymal transition (EMT) by recruiting SMARCA4/BRG1. Represses BCL6 transcription in the presence of the corepressor CTBP1. Positively regulates neuronal differentiation. Represses RCOR1 transcription activation during neurogenesis. Represses transcription by binding to the E box (5'-CANNTG-3'). Promotes tumorigenicity by repressing stemness-inhibiting microRNAs.
Chromosomal Localization:
2q22.3
Accession Number:
NP_001165124
UniProt Accession Number:
O60315
DNA Source:
The NCI acknowledges the generous advice and gene clones provided by Robert A. Weinberg at the Ludwig Center for Cancer Research of the Massachusetts Institute of Technology. These reagents have been provided by the Division of Cancer Treatment and Diagnosis (DCTD) of the National Cancer Institute (NCI) using funding of the American Recovery and Reinvestment Act of 2009
Immunogen:
Synthetic Peptide
Vector Name:
N/A
Extinction Coefficient:
Buffers:
Expressed Sequence:
cEELQAEPLDLSLPKQMKEP
Native Sequence:
Calculated Isoelectric Point:
0
Molecular Weight:
2090
Last Updated:
09/16/2019
No SOPs available.
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