ARG11088

anti-Nurr1 antibody

anti-Nurr1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes Nurr1
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name Nurr1
Antigen Species Human
Immunogen Synthetic peptide corresponding to aa. 566-591 of Human Nurr1. (CTQGL QRIFY LKLED LVPPP AIIDK L)
Conjugation Un-conjugated
Alternate Names TINUR; Orphan nuclear receptor NURR1; NURR1; Immediate-early response protein NOT; HZF-3; Transcriptionally-inducible nuclear receptor; NOT; Nuclear receptor subfamily 4 group A member 2; RNR1

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1:50 - 1:100
WB1:500
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Observed Size 65 - 75 kDa

Properties

Form Liquid
Purification Affinity purified.
Buffer Tris, HCl/Glycine buffer (pH 7.4-7.8), cryo-protective agents, Hepes, 0.02% Sodium azide, 30% Glycerol and 0.5% BSA.
Preservative 0.02% Sodium azide
Stabilizer 30% Glycerol and 0.5% BSA
Concentration 0.61 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 18227 Mouse NR4A2

GeneID: 4929 Human NR4A2

Swiss-port # P43354 Human Nuclear receptor subfamily 4 group A member 2

Swiss-port # Q06219 Mouse Nuclear receptor subfamily 4 group A member 2

Gene Symbol NR4A2
Gene Full Name nuclear receptor subfamily 4, group A, member 2
Background This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcription factor. Mutations in this gene have been associated with disorders related to dopaminergic dysfunction, including Parkinson disease, schizophernia, and manic depression. Misregulation of this gene may be associated with rheumatoid arthritis. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Function Transcriptional regulator which is important for the differentiation and maintenance of meso-diencephalic dopaminergic (mdDA) neurons during development. It is crucial for expression of a set of genes such as SLC6A3, SLC18A2, TH and DRD2 which are essential for development of mdDA neurons (By similarity). [UniProt]
Cellular Localization Cytoplasm. Nucleus. Note=Mostly nuclear; oxidative stress promotes cytoplasmic localization. [UniProt]
Calculated MW 67 kDa