Product Name
NR2E3, Blocking Peptide
Full Product Name
NR2E3 Peptide
Product Gene Name
NR2E3 blocking peptide
[Similar Products]
Product Synonym Gene Name
PNR; RNR; rd7; ESCS; RP37[Similar Products]
NR2E3 peptide (MBS3229389) is used for blocking the activity of NR2E3 antibody (MBS3204422)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q9Y5X4
Form/Format
Lyophilized powder
Preparation and Storage
Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.
Other Notes
Small volumes of NR2E3 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
NR2E3 blocking peptide
This is a synthetic peptide designed for use in combination with anti-NR2E3 antibody made
Target Description: NR2E3 is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in *****s. NR2E3 is a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome.This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in *****s. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
Product Categories/Family for NR2E3 blocking peptide
Peptide
Applications Tested/Suitable for NR2E3 blocking peptide
Western Blot (WB)
NCBI/Uniprot data below describe general gene information for NR2E3. It may not necessarily be applicable to this product.
NCBI Accession #
NP_055064
[Other Products]
NCBI GenBank Nucleotide #
NM_014249
[Other Products]
UniProt Primary Accession #
Q9Y5X4
[Other Products]
UniProt Related Accession #
Q9Y5X4[Other Products]
NCBI Official Full Name
photoreceptor-specific nuclear receptor isoform b
NCBI Official Synonym Full Names
nuclear receptor subfamily 2 group E member 3
NCBI Official Symbol
NR2E3 [Similar Products]
NCBI Official Synonym Symbols
PNR; RNR; rd7; ESCS; RP37
[Similar Products]
NCBI Protein Information
photoreceptor-specific nuclear receptor
UniProt Protein Name
Photoreceptor-specific nuclear receptor
UniProt Synonym Protein Names
Nuclear receptor subfamily 2 group E member 3; Retina-specific nuclear receptor
Protein Family
Photoreceptor-specific nuclear receptor
UniProt Gene Name
NR2E3 [Similar Products]
UniProt Synonym Gene Names
PNR; RNR [Similar Products]
UniProt Entry Name
NR2E3_HUMAN
NCBI Summary for NR2E3
This protein is part of a large family of nuclear receptor transcription factors involved in signaling pathways. Nuclear receptors have been shown to regulate pathways involved in embryonic development, as well as in maintenance of proper cell function in *****s. Members of this family are characterized by discrete domains that function in DNA and ligand binding. This gene encodes a retinal nuclear receptor that is a ligand-dependent transcription factor. Defects in this gene are a cause of enhanced S cone syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]
UniProt Comments for NR2E3
NR2E3: Orphan nuclear receptor of retinal photoreceptor cells. Transcriptional factor that is an activator of rod development and repressor of cone development. Binds the promoter region of a number of rod- and cone-specific genes, including rhodopsin, M- and S-opsin and rod-specific phosphodiesterase beta subunit. Enhances rhodopsin expression. Represses M- and S-cone opsin expression. Defects in NR2E3 are a cause of enhanced S cone syndrome (ESCS). ESCS is an autosomal recessive retinopathy in which patients have increased sensitivity to blue light; perception of blue light is mediated by what is normally the least populous cone photoreceptor subtype, the S (short wavelength, blue) cones. ESCS is also associated with visual loss, with night blindness occurring from early in life, varying degrees of L (long, red)- and M (middle, green)-cone vision, and retinal degeneration. Defects in NR2E3 are the cause of retinitis pigmentosa type 37 (RP37). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP37 inheritance is autosomal dominant. Belongs to the nuclear hormone receptor family. NR2 subfamily. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Nuclear receptor
Chromosomal Location of Human Ortholog: 15q23
Cellular Component: nucleoplasm; transcription factor complex; nucleus
Molecular Function: protein binding; ligand-dependent nuclear receptor activity; zinc ion binding; sequence-specific DNA binding; steroid hormone receptor activity
Biological Process: transcription from RNA polymerase II promoter; transcription initiation from RNA polymerase II promoter; intracellular receptor-mediated signaling pathway; positive regulation of rhodopsin gene expression; negative regulation of transcription from RNA polymerase II promoter; signal transduction; negative regulation of cell proliferation; eye photoreceptor cell development; visual perception; retina development in camera-type eye; phototransduction; steroid hormone mediated signaling; gene expression; positive regulation of transcription from RNA polymerase II promoter
Disease: Retinitis Pigmentosa 37; Enhanced S-cone Syndrome
Research Articles on NR2E3
1. Macular involvement was detectable in all the patients, and the abnormal foveal avascular zone (FAZ) supports the role of NR2E3 in retinal development.
Precautions
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Disclaimer
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