Anti-Phospho-Ah Receptor-Ser36 antibody (2-51 aa) (STJ90873)

SPECIFICATIONS
ClonalityPolyclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
ImmunogenThe antiserum was produced against synthesized peptide derived from the human AhR around the phosphorylation site of Ser36 at the amino acid range 2-51
STJ90873
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General Information

Short DescriptionRabbit polyclonal anti-Phospho-Aryl hydrocarbon receptor and Aryl hydrocarbon receptor repressor-Ser36 (2-51 aa) for use in WB, IHC, IF and ELISA in Human, Mouse and Rat samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsWB/IHC/IF/ELISA
HostRabbit
ReactivityHuman/Mouse/Rat
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityPolyclonal
IsotypeIgG
ConjugationUnconjugated
Concentration1 mg/mL
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Dilution RangeWB 1:500-1:2000
IHC 1:100-1:300
ELISA 1:5000
IF 1:50-200
FormulationLiquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide.
Storage InstructionStore at-20°C for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.

Target Information

Gene SymbolAHRR
AHR
Gene ID57491
196
Uniprot IDAHRR_HUMAN
AHR_HUMAN
ImmunogenThe antiserum was produced against synthesized peptide derived from the human AhR around the phosphorylation site of Ser36 at the amino acid range 2-51
Immunogen Region2-51 aa
SpecificityPhospho-Ah Receptor (S36) Polyclonal Antibody detects endogenous levels of Ah Receptor protein only when phosphorylated at S36.

Additional Info

Post Translational Modifications Mono-ADP-ribosylated, leading to inhibit transcription activator activity of AHR.
Function Ligand-activated transcription factor that enables cells to adapt to changing conditions by sensing compounds from the environment, diet, microbiome and cellular metabolism, and which plays important roles in development, immunity and cancer. Upon ligand binding, translocates into the nucleus, where it heterodimerizes with ARNT and induces transcription by binding to xenobiotic response elements (XRE). Regulates a variety of biological processes, including angiogenesis, hematopoiesis, drug and lipid metabolism, cell motility and immune modulation. Xenobiotics can act as ligands: upon xenobiotic-binding, activates the expression of multiple phase I and II xenobiotic chemical metabolizing enzyme genes (such as the CYP1A1 gene). Mediates biochemical and toxic effects of halogenated aromatic hydrocarbons. Next to xenobiotics, natural ligands derived from plants, microbiota, and endogenous metabolism are potent AHR agonists. Tryptophan (Trp) derivatives constitute an important class of endogenous AHR ligands. Acts as a negative regulator of anti-tumor immunity: indoles and kynurenic acid generated by Trp catabolism act as ligand and activate AHR, thereby promoting AHR-driven cancer cell motility and suppressing adaptive immunity. Regulates the circadian clock by inhibiting the basal and circadian expression of the core circadian component PER1. Inhibits PER1 by repressing the CLOCK-ARNTL/BMAL1 heterodimer mediated transcriptional activation of PER1. The heterodimer ARNT:AHR binds to core DNA sequence 5'-TGCGTG-3' within the dioxin response element (DRE) of target gene promoters and activates their transcription.
Protein Name Aryl Hydrocarbon Receptor
Ah Receptor
Ahr
Class E Basic Helix-Loop-Helix Protein 76
Bhlhe76
Database Links Reactome: R-HSA-1989781
Reactome: R-HSA-211945
Reactome: R-HSA-211976
Reactome: R-HSA-211981
Reactome: R-HSA-8937144
Cellular Localisation Cytoplasm
Nucleus
Initially Cytoplasmic
Upon Binding With Ligand And Interaction With A Hsp90
It Translocates To The Nucleus
Alternative Antibody Names Anti-Aryl Hydrocarbon Receptor antibody
Anti-Ah Receptor antibody
Anti-Ahr antibody
Anti-Class E Basic Helix-Loop-Helix Protein 76 antibody
Anti-Bhlhe76 antibody
Anti-AHR antibody
Anti-BHLHE76 antibody

Information sourced from Uniprot.org

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