NR4A2
(Nuclear Receptor Subfamily 4, Group A, Member 2 (NR4A2))
宿主
人
资源
合成
应用范围
Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
产品特性
This is a synthetic peptide designed for use in combination with anti-NR4A2 antibody (Catalog #: ARP38753_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
Each Investigator should determine their own optimal working dilution for specific applications.
限制
仅限研究用
状态
Lyophilized
溶解方式
Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
浓度
1 mg/mL
缓冲液
Final peptide concentration is 1 mg/mL in PBS.
注意事项
Avoid repeated freeze-thaw cycles.
储存条件
-20 °C
储存方法
For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
抗原
NR4A2
(Nuclear Receptor Subfamily 4, Group A, Member 2 (NR4A2))
别名
nr41/42/43 Peptide, Nr4a2 Peptide, nurr1 Peptide, not Peptide, rnr1 Peptide, hzf-3 Peptide, tinur Peptide, NGFI-B Peptide, HZF-3 Peptide, NOT Peptide, NURR1 Peptide, RNR1 Peptide, TINUR Peptide, Nurr1 Peptide, RNR-1 Peptide, TINOR Peptide, ngf1b Peptide, nr4a2 Peptide, zgc:92696 Peptide, nuclear receptor subfamily 4 group A member 2 Peptide, nuclear receptor Peptide, nuclear receptor subfamily 4, group A, member 2 Peptide, nuclear receptor subfamily 4, group A, member 2b Peptide, NR4A2 Peptide, nr41/42/43 Peptide, nr4a2 Peptide, Nr4a2 Peptide, nr4a2b Peptide
背景
NR4A2 is a member of the steroid-thyroid hormone-retinoid receptor superfamily. The protein may act as a transcription factor. Mutations in NR4A2 gene have been associated with disorders related to dopaminergic dysfunction, including Parkinson disease, schizophernia, and manic depression. Misregulation of NR4A2 gene may be associated with rheumatoid arthritis.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. Four transcript variants encoding four distinct isoforms have been identified for this gene. Additional alternate splice variants may exist, but their full length nature has not been determined.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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: HZF-3, NOT, NURR1, RNR1, TINUR
Protein Interaction Partner: CREB1,CDKN1C,COPS5,PIAS4,RPS6KA1,RXRA,RXRB,RARA,RARB