Anti-Recombinant-DOK1 antibody [RM2RM24] (STJA0026483)

SPECIFICATIONS
ClonalityMonoclonal
HostRabbit
ConjugationUnconjugated
IsotypeIgG
STJA0026483
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General Information

Short DescriptionRabbit monoclonal anti-Recombinant-Docking Protein 1 for use in IF and WB in Human, Mouse and Rat samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsIF/WB
HostRabbit
ReactivityHuman/Mouse/Rat
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone IDRM2RM24
IsotypeIgG
ConjugationUnconjugated
PurificationProtein A/G purified from cell culture supernatant
Dilution RangeIF: 1:50-1:200, WB: 1:1000-1:2000
Formulation0.01M PBS, pH 7.4, 0.05% BSA, 50% Glycerol, 0.05% Sodium Azide
Storage InstructionSuitable for storage at +4°C between 1-2 weeks. For longer term store at-20°C for up to 12 months.

Target Information

Gene SymbolDOK1
Gene ID1796
Uniprot IDDOK1_HUMAN

Additional Info

Post Translational Modifications Constitutively tyrosine-phosphorylated. Phosphorylated by TEC. Phosphorylated by LYN. Phosphorylated on tyrosine residues by the insulin receptor kinase. Results in the negative regulation of the insulin signaling pathway. Phosphorylated on tyrosine residues by SRMS.
Function DOK proteins are enzymatically inert adaptor or scaffolding proteins. They provide a docking platform for the assembly of multimolecular signaling complexes. DOK1 appears to be a negative regulator of the insulin signaling pathway. Modulates integrin activation by competing with talin for the same binding site on ITGB3.
Protein Name Docking Protein 1
Downstream Of Tyrosine Kinase 1
P62(Dok
Pp62
Database Links Reactome: R-HSA-8849469
Reactome: R-HSA-8853659
Cellular Localisation Isoform 1: Cytoplasm
Nucleus
Isoform 3: Cytoplasm
Perinuclear Region
Alternative Antibody Names Anti-Docking Protein 1 antibody
Anti-Downstream Of Tyrosine Kinase 1 antibody
Anti-P62(Dok antibody
Anti-Pp62 antibody
Anti-DOK1 antibody

Information sourced from Uniprot.org

Citations

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