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Zinc finger E-box-binding homeobox

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Acts as a transcriptional repressor. Positively regulates neuronal differentiation. Represses transcription by binding to the E box-containing promoter (By similarity). Binds to delta 1-crystallin enhancer core and represses lens-specific transcription. It binds as well many other non-lens specific DNA sequences.

Below are the list of possible Zinc finger E-box-binding homeobox products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Zinc finger E-box-binding homeobox 1

 Zinc finger E-box-binding homeobox 1 ELISA Kit
 Zinc finger E-box-binding homeobox 1 Recombinant
 Zinc finger E-box-binding homeobox 1 Antibody
Also known as Zinc finger E-box-binding homeobox 1 (Delta EF1) (Delta-crystallin enhancer-binding factor) (Transcription factor 8) (TCF-8).
Acts as a transcriptional repressor. Positively regulates neuronal differentiation. Represses transcription by binding to the E box-containing promoter (). Binds to delta 1-crystallin enhancer core and represses lens-specific transcription. It binds as well
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many other non-lens specific DNA sequences.
 ZEB1 ELISA Kit
 ZEB1 Recombinant
 ZEB1 Antibody
 TCF8 ELISA Kit
 TCF8 Recombinant
 TCF8 Antibody
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Zinc finger E-box-binding homeobox 2

 Zinc finger E-box-binding homeobox 2 ELISA Kit
 Zinc finger E-box-binding homeobox 2 Recombinant
 Zinc finger E-box-binding homeobox 2 Antibody
Also known as Zinc finger E-box-binding homeobox 2 (Smad-interacting protein 1) (SMADIP1) (Zinc finger homeobox protein 1b).
ZEB2: Transcriptional inhibitor that binds to DNA sequence 5'- CACCT-3' in different promoters. Represses transcription of E- cadherin. Defects in ZEB2 are the cause of Mowat-Wilson syndrome (MWIS); also known as Hirschsprung disease-mental retardation syndrome. A complex developmental disorder characterized by mental retardation, delayed motor development, epilepsy, microcephaly and a wide spectrum of clinically heterogeneous features suggestive of neurocristopathies
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at the cephalic, cardiac, and vagal levels. Some patients manifest Hirschsprung disease. Affected patients show an easily recognizable facial appearance with deep set eyes and hypertelorism, medially divergent, broad eyebrows, prominent columella, pointed chin and uplifted, notched ear lobes. Belongs to the delta-EF1/ZFH-1 C2H2-type zinc-finger family.

Protein type: C2H2-type zinc finger protein; DNA-binding; Motility/polarity/chemotaxis; Transcription, coactivator/corepressor

Chromosomal Location of Human Ortholog: 2q22.3

Cellular Component: nucleus

Molecular Function: protein binding

Biological Process: negative regulation of transcription from RNA polymerase II promoter; pigmentation during development; positive regulation of melanin biosynthetic process; positive regulation of melanocyte differentiation; positive regulation of transcription from RNA polymerase II promoter

Disease: Mowat-wilson Syndrome
 ZEB2 ELISA Kit
 ZEB2 Recombinant
 ZEB2 Antibody
 KIAA0569 ELISA Kit
 KIAA0569 Recombinant
 KIAA0569 Antibody
 SIP1 ELISA Kit
 SIP1 Recombinant
 SIP1 Antibody
 ZFHX1B ELISA Kit
 ZFHX1B Recombinant
 ZFHX1B Antibody
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