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.
Beschränkungen
Nur für Forschungszwecke einsetzbar
Format
Lyophilized
Rekonstitution
Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
Konzentration
1 mg/mL
Buffer
Antibody is lyophilized in PBS buffer with 2 % sucrose.
Handhabung
As with any antibody avoid repeat freeze-thaw cycles.
Lagerung
4 °C/-20 °C
Informationen zur Lagerung
For short periods of storage (days) store at 4 °C. For longer periods of storage, store NR2E3 antibody at -20 °C.
Target
NR2E3
(Nuclear Receptor Subfamily 2, Group E, Member 3 (NR2E3))
ESCS antikoerper, PNR antikoerper, RNR antikoerper, RP37 antikoerper, rd7 antikoerper, LOC100228348 antikoerper, A930035N01Rik antikoerper, wu:fj55b07 antikoerper, zgc:103631 antikoerper, nuclear receptor subfamily 2 group E member 3 antikoerper, nuclear receptor subfamily 2, group E, member 3 antikoerper, NR2E3 antikoerper, Nr2e3 antikoerper, nr2e3 antikoerper
Hintergrund
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.