NOR-1 rabbit pAb

NOR-1 rabbit pAb

AO-06-ES7612-50

NOR-1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES7612
Product nameNOR-1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameNR4A3; CHN; CSMF; MINOR; NOR1; TEC; Nuclear receptor subfamily 4 group A member 3; Mitogen-induced nuclear orphan receptor; Neuron-derived orphan receptor 1; Nuclear hormone receptor NOR-1
Size50μL
Unit price ($)148
Human gene ID8013
Human Swiss-ProtQ92570
SourceRabbit
IsotypeIgG
TargetNOR-1
Fields>>Transcriptional misregulation in cancer
Gene nameNR4A3
Protein nameNuclear receptor subfamily 4 group A member 3
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18124
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9QZB6
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID58853
Rat gene linkView Rat Gene
Rat Swiss-ProtP51179
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human NR4A3. AA range:387-436
SpecificityNOR-1 Polyclonal Antibody detects endogenous levels of NOR-1 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)65kD
BackgroundThis gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. The encoded protein may act as a transcriptional activator. The protein can efficiently bind the NGFI-B Response Element (NBRE). Three different versions of extraskeletal myxoid chondrosarcomas (EMCs) are the result of reciprocal translocations between this gene and other genes. The translocation breakpoints are associated with Nuclear Receptor Subfamily 4, Group A, Member 3 (on chromosome 9) and either Ewing Sarcome Breakpoint Region 1 (on chromosome 22), RNA Polymerase II, TATA Box-Binding Protein-Associated Factor, 68-KD (on chromosome 17), or Transcription factor 12 (on chromosome 15). Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010],
Functiondisease:A chromosomal aberration involving NR4A3 is a cause of a form of extraskeletal myxoid chondrosarcomas (EMC). Translocation t(9;17)(q22;q11) with TAF2N.,disease:A chromosomal aberration involving NR4A3 is a cause of Ewing sarcoma [MIM:133450]. Translocation t(9;22)(q22-31;q11-12) with EWS.,function:Binds to the B1A response-element.,similarity:Belongs to the nuclear hormone receptor family.,similarity:Belongs to the nuclear hormone receptor family. NR4 subfamily.,similarity:Contains 1 nuclear receptor DNA-binding domain.,tissue specificity:High expression of isoform alpha in skeletal muscle. High expression of isoform beta in skeletal muscle and low expression in fetal brain and placenta.,
Subcellular locationNucleus .
ExpressionIsoform alpha is highly expressed in skeletal muscle. Isoform beta is highly expressed in skeletal muscle and low expressed in fetal brain and placenta.

Additional Images

Image 1
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Western blot analysis of lysates from COLO cells, using NR4A3 Antibody. The lane on the right is blocked with the synthesized peptide.
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: AO-06-ES7612-50
: 10 Items
Hurry! only 10 items left in stock.

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