TRAF2 Rabbit Polyclonal Antibody

SKU
TA319201
Anti-TRAF2 (RABBIT) Antibody, 100 ug
  $870.00
5 Days*
Bulk/Customize
Specifications
Specifications
Product Data
Application ELISA, IF, WB
Recommended Dilution WB: 1 µg/mL
IF: User Optimized
ELISA: 1:60,000 - 1:250,000
Reactivity Human
Antibody Host Rabbit
Isotype IgG
Clonality Polyclonal
Immunogen This affinity purified antibody was prepared from whole rabbit serum produced by repeated immunizations with a synthetic peptide corresponding to an internal region human TRAF2.
Specificity This affinity purified antibody is directed against human TRAF2 protein. The product was affinity purified from monospecific antiserum by immunoaffinity chromatography. This antibody is predicted to react with TRAF2 from human and mouse sources based on a 100% homology with the immunizing sequence. Reactivity with TRAF2 from other sources has not been determined.
Buffer 0.02 M Potassium Phosphate, 0.15 M Sodium Chloride, pH 7.2
Stabilizer: None
Preservative: 0.01% (w/v) Sodium Azide
Concentration 0.93 mg/mL - lot specific
Conjugation Unconjugated
Storage Store vial at -20° C prior to opening. Aliquot contents and freeze at -20° C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. This product is stable for several weeks at 4° C as an undiluted liquid. Dilute only prior to immediate use.
Stability Expiration date is one (1) year from date of receipt.
Shipping Blue Ice
Gene Name TNF receptor associated factor 2
Database Link
Background TRAF2, or Tumor Necrosis factor (TNF) Receptor-Associated Factor 2, is an adapter protein and signal transducer that links members of the tumor necrosis factor receptor family to different signaling pathways by association with the receptor cytoplasmic domain and kinases. Association to the receptor is also mediated by the interaction with TRADD. TRAF2 mediates activation of NF-kappa-B and MAPK8/JNK and is involved in apoptosis. TRAF2 forms a heterodimeric complex with TRAF1, which then recruits the inhibitor-of-apoptosis proteins (IAPs), apoptotic suppressors BIRC2 and BIRC3 to TNFRSF1B/TNFR2 for the inhibition of caspase activation. In this way it functions as a mediator of the anti-apoptotic signals from TNF receptors. BIRC2/c-IAP1, an apoptosis inhibitor possessing ubiquitin ligase activity, can unbiquitinate and induce the degradation of this protein, and thus potentiate TNF-induced apoptosis. TRAF2 may be involved in IL-15 signaling. Multiple alternatively spliced transcript variants exist, but the biological validity of only one transcript has been determined.
Synonyms rabbit anti-TRAF2 antibody, E3 ubiquitin-protein ligase TRAF2, RING-type E3 ubiquitin transferase TRAF2, TNF receptor associated factor 2 antibody, TRAF-2, TRAF 2 antibody, TRAP-3, TRAP 3 antibody, TRAP3 antibody, Tumor necrosis factor type 2 receptor associated protein 3 antibody
Note Rabbit Anti-TRAF2 Antibody has been tested in ELISA and Western Blot. Positive control HeLa Whole Cell lysate (p/n W09-000-364) expect ~47kDa. Specific conditions for reactivity should be optimized by the end user.
Reference Data
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file-alt Citations

RIG-I Promotes Cell Death in Hepatocellular Carcinoma by Inducing M1 Polarization of Perineal Macrophages Through the RIG-I/MAVS/NF-κB Pathway
Zhou, Li, Yang et al
OncoTargets and therapy (2020) 13, 8783-8794 DOI: 10.2147/OTT.S258450
AI Summary: OriGene products, including the Ddx58 (NM_172689) Mouse Tagged ORF Clone Lentiviral Particle (CAT#: MR226477L4V), Lenti ORF control particles of pLenti-C-mGFP-P2A-Puro (CAT#: PS100093V), and TA310155, were used for RIG-I overexpression and as experimental controls to investigate the role of RIG-I in macrophage polarization and hepatocellular carcinoma cell death.
Snippet: Ddx58 (NM_172689) Mouse Tagged ORF Clone Lentiviral Particle (CAT#: MR226477L4V) and Lenti ORF control particles of pLenti-C-mGFP-P2A-Puro (CAT#: PS100093V) were purchased from Origene Corporation No. TA310155) was obtained from OriGene
FigureFigureFigure
WB FC
Showing 1-1 of 1 papers.
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