Anti-TAB1 antibody (N-Term) [3D10-G10-B6] (STJ99124)

SPECIFICATIONS
ClonalityMonoclonal
HostMouse
ConjugationUnconjugated
ImmunogenPurified recombinant human TAB1 (N-terminus) protein fragments expressed in E.coli.
STJ99124
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General Information

Short DescriptionMouse monoclonal anti-TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 (N-Term) for use in WB in Human samples. Datasheet included with dilution recommendations, and related reagents.
ApplicationsWB
HostMouse
ReactivityHuman
NoteSTRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.

Product Properties

ClonalityMonoclonal
Clone ID3D10-G10-B6
ConjugationUnconjugated
Concentration1 mg/mL
PurificationThe antibody was affinity-purified from mouse ascites by affinity-chromatography using epitope-specific immunogen.
Dilution RangeWB 1:1000
FormulationLiquid in PBS containing 50% Glycerol, 0.5% BSA and 0.02% Sodium Azide.
Storage InstructionStore at-20ยฐC for up to 1 year from the date of receipt, and avoid repeat freeze-thaw cycles.

Target Information

Gene SymbolTAB1
Gene ID10454
Uniprot IDTAB1_HUMAN
ImmunogenPurified recombinant human TAB1 (N-terminus) protein fragments expressed in E.coli.
Immunogen RegionN-Term
SpecificityThis antibody detects endogenous levels of TAB1 (N-terminus) and does not cross-react with related proteins.

Additional Info

Post Translational Modifications Phosphorylated at all three sites Ser-423, Thr-431 and Ser-438 by MAPK14 when cells were exposed to cellular stresses, or stimulated with TNF-alpha, IL1 or LPS. These phosphorylations inhibit TAK1 activation by a feedback control mechanism. Dephosphorylated by DUSP14 at Ser-438, leading to TAB1-MAP3K7/TAK1 complex inactivation in T-cells. Ubiquitinated by MAP3K1 with 'Lys-63'-linked polyubiquitin.leading to activation of TAK1 and of JNK and p38 MAP kinases following EGF and TGF-beta stimulation. Ubiquitinated by ITCH with 'Lys-48'-linked polyubiquitin.leading to proteasomal degradation. Ubiquitinated by RNF114 during maternal-to-zygotic transition.leading to degradation. (Microbial infection) Deubiquitinated by Y.enterocolitica YopP. O-GlcNAcylated at Ser-395 by OGT is required for full MAP3K7/TAK1 activation upon stimulation with IL-1 or osmotic stress. Deglycosylated at Ser-395 by OGA.
Function Key adapter protein that plays an essential role in JNK and NF-kappa-B activation and proinflammatory cytokines production in response to stimulation with TLRs and cytokines. Mechanistically, associates with the catalytic domain of MAP3K7/TAK1 to trigger MAP3K7/TAK1 autophosphorylation leading to its full activation. Similarly, associates with MAPK14 and triggers its autophosphorylation and subsequent activation. In turn, MAPK14 phosphorylates TAB1 and inhibits MAP3K7/TAK1 activation in a feedback control mechanism. Also plays a role in recruiting MAPK14 to the TAK1 complex for the phosphorylation of the TAB2 and TAB3 regulatory subunits.
Protein Name Tgf-Beta-Activated Kinase 1 And Map3k7-Binding Protein 1
Mitogen-Activated Protein Kinase Kinase Kinase 7-Interacting Protein 1
Tgf-Beta-Activated Kinase 1-Binding Protein 1
Tak1-Binding Protein 1
Database Links Reactome: R-HSA-168638
Reactome: R-HSA-2871837
Reactome: R-HSA-445989
Reactome: R-HSA-450302
Reactome: R-HSA-450321
Reactome: R-HSA-5357956
Reactome: R-HSA-5607764
Reactome: R-HSA-5689880
Reactome: R-HSA-9014325
Reactome: R-HSA-9020702
Reactome: R-HSA-937042
Reactome: R-HSA-937072
Reactome: R-HSA-9645460
Reactome: R-HSA-9705671
Reactome: R-HSA-975163
Cellular Localisation Cytoplasm
Cytosol
Endoplasmic Reticulum Membrane
Peripheral Membrane Protein
Cytoplasmic Side
Recruited To The Endoplasmic Reticulum Following Interaction With Sting1
Alternative Antibody Names Anti-Tgf-Beta-Activated Kinase 1 And Map3k7-Binding Protein 1 antibody
Anti-Mitogen-Activated Protein Kinase Kinase Kinase 7-Interacting Protein 1 antibody
Anti-Tgf-Beta-Activated Kinase 1-Binding Protein 1 antibody
Anti-Tak1-Binding Protein 1 antibody
Anti-TAB1 antibody
Anti-MAP3K7IP1 antibody

Information sourced from Uniprot.org

Citations

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