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Tax1 binding protein 1 Monoclonal Antibody + Cell Lysate Kit

Applications

  • WB
  • FCM
  • IC

Reactivity

  • Human
  • Mouse
  • Rat
Overview
Catalog # bsm-90018R
Product Name Tax1 binding protein 1 Monoclonal Antibody + Cell Lysate Kit
Applications WB, FCM, IC
Specificity Knockdown Validated
Reactivity Human, Mouse, Rat
Specifications
Conjugation Unconjugated
Host Rabbit
Source A synthesized peptide derived from human TRAF6BP
Immunogen Range 720-789/789
Clonality Monoclonal
Clone # 23GB2100
Isotype IgG
Concentration Lot dependent
Purification Affinity Purified
Storage Buffer Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.
Storage Condition -20 °C
Target
Gene ID 8887
Swiss Prot Q86VP1
Synonyms TAX1BP1; Tax1 Binding Protein 1; CALCOCO3; TXBP151; Tax1 (Human T-Cell Leukemia Virus Type I) Binding Protein 1; Tax1-Binding Protein 1; TRAF6-Binding Protein; T6BP
Background Ubiquitin-binding adapter that participates in inflammatory, antiviral and innate immune processes as well as selective autophagy regulation. Plays a key role in the negative regulation of NF-kappa-B and IRF3 signalings by acting as an adapter for the ubiquitin-editing enzyme A20/TNFAIP3 to bind and inactivate its substrates. Disrupts the interactions between the E3 ubiquitin ligase TRAF3 and TBK1/IKBKE to attenuate 'Lys63'-linked polyubiquitination of TBK1 and thereby IFN-beta production. Recruits also A20/TNFAIP3 to ubiquitinated signaling proteins TRAF6 and RIPK1, leading to their deubiquitination and disruption of IL-1 and TNF-induced NF-kappa-B signaling pathways. Inhibits virus-induced apoptosis by inducing the 'Lys-48'-linked polyubiquitination and degradation of MAVS via recruitment of the E3 ligase ITCH, thereby attenuating MAVS-mediated apoptosis signaling. As a macroautophagy/autophagy receptor, facilitates the xenophagic clearance of pathogenic bacteria such as Salmonella typhimurium and Mycobacterium tuberculosis. Upon NBR1 recruitment to the SQSTM1-ubiquitin condensates, acts as the major recruiter of RB1CC1 to these ubiquitin condensates to promote their autophagic degradation. Mediates the autophagic degradation of other substrates including TICAM1.

Cell Line: HeLa

Knockdown technology: shRNA Knockdown
Application Dilution
WB : 1:1000-1:5000
FCM FCM: 1:2000
IC IC: 1:1000