NR2E3
Reactivité: Humain, Souris, Rat, Boeuf (Vache), Porc
WB
Hôte: Lapin
Polyclonal
unconjugated
Indications d'application
NR2E3 antibody can be used for detection of NR2E3 by ELISA at 1:312500. NR2E3 antibody can be used for detection of NR2E3 by western blot at 1.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Restrictions
For Research Use only
Format
Lyophilized
Reconstitution
Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Concentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Conseil sur la manipulation
As with any antibody avoid repeat freeze-thaw cycles.
Stock
4 °C/-20 °C
Stockage commentaire
For short periods of storage (days) store at 4 °C. For longer periods of storage, store NR2E3 antibody at -20 °C.
Antigène
NR2E3
(Nuclear Receptor Subfamily 2, Group E, Member 3 (NR2E3))
anticorps ESCS, anticorps PNR, anticorps RNR, anticorps RP37, anticorps rd7, anticorps LOC100228348, anticorps A930035N01Rik, anticorps wu:fj55b07, anticorps zgc:103631, anticorps nuclear receptor subfamily 2 group E member 3, anticorps nuclear receptor subfamily 2, group E, member 3, anticorps NR2E3, anticorps Nr2e3, anticorps nr2e3
Sujet
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 adults. 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 adults. 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.