Anti-NFkB p105 / p50 antibody (ab75728)

Overview

• Product nameAnti-NFkB p105 / p50 antibodySee all NFkB p105 / p50 primary antibodies ...
• Description
  Rabbit polyclonal to NFkB p105 / p50
• Tested applicationsWB, ELISA more details
• Species reactivity
  Reacts with: Human
  
• Immunogen

  Synthetic peptide (Human) surrounding S903 conjugated to KLH

• Positive controlSK-BR-3 cell lysate

Properties

• FormLiquid
• Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
• Storage bufferPreservative: 0.09% Sodium Azide
  Constituents: PBS
• Concentration information loading...
• PurityProtein G purified
• Purification notesThis antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
• Clonality Polyclonal
• IsotypeIgG
• Research Areas
  • Cancer
  • Signal transduction
  • Nuclear signaling
  • NFkB pathway

  • Signal Transduction
  • Signaling Pathway
  • Nuclear Signaling
  • NFkB Pathway

  • Other Factors

  • Epigenetics and Nuclear Signaling
  • Transcription
  • Transcription Factors

  • Epigenetics and Nuclear Signaling
  • Nuclear Signaling Pathways
  • NFkB pathway

  • Immunology
  • Innate Immunity
  • Macrophage / Inflamm.

  • Cell Biology
  • Apoptosis
  • Intracellular
  • NFkB
  • p50

Applications

Target

• FunctionNF-kappa-B is a pleiotropic transcription factor which is present in almost all cell types and is involved in many biological processed such as inflammation, immunity, differentiation, cell growth, tumorigenesis and apoptosis. NF-kappa-B is a homo- or heterodimeric complex formed by the Rel-like domain-containing proteins RELA/p65, RELB, NFKB1/p105, NFKB1/p50, REL and NFKB2/p52 and the heterodimeric p65-p50 complex appears to be most abundant one. The dimers bind at kappa-B sites in the DNA of their target genes and the individual dimers have distinct preferences for different kappa-B sites that they can bind with distinguishable affinity and specificity. Different dimer combinations act as transcriptional activators or repressors, respectively. NF-kappa-B is controlled by various mechanisms of post-translational modification and subcellular compartmentalization as well as by interactions with other cofactors or corepressors. NF-kappa-B complexes are held in the cytoplasm in an inactive state complexed with members of the NF-kappa-B inhibitor (I-kappa-B) family. In a conventional activation pathway, I-kappa-B is phosphorylated by I-kappa-B kinases (IKKs) in response to different activators, subsequently degraded thus liberating the active NF-kappa-B complex which translocates to the nucleus. NF-kappa-B heterodimeric p65-p50 and RelB-p50 complexes are transcriptional activators. The NF-kappa-B p50-p50 homodimer is a transcriptional repressor, but can act as a transcriptional activator when associated with BCL3. NFKB1 appears to have dual functions such as cytoplasmic retention of attached NF-kappa-B proteins by p105 and generation of p50 by a cotranslational processing. The proteasome-mediated process ensures the production of both p50 and p105 and preserves their independent function, although processing of NFKB1/p105 also appears to occur post-translationally. p50 binds to the kappa-B consensus sequence 5'-GGRNNYYCC-3', located in the enhancer region of genes involved in immune response and acute phase reactions. In a complex with MAP3K8, NFKB1/p105 represses MAP3K8-induced MAPK signaling; active MAP3K8 is released by proteasome-dependent degradation of NFKB1/p105.
• Sequence similaritiesContains 7 ANK repeats.
  Contains 1 death domain.
  Contains 1 RHD (Rel-like) domain.
• DomainThe C-terminus of p105 might be involved in cytoplasmic retention, inhibition of DNA-binding, and transcription activation.
  Glycine-rich region (GRR) appears to be a critical element in the generation of p50.
• Post-translational
  modificationsWhile translation occurs, the particular unfolded structure after the GRR repeat promotes the generation of p50 making it an acceptable substrate for the proteasome. This process is known as cotranslational processing. The processed form is active and the unprocessed form acts as an inhibitor (I kappa B-like), being able to form cytosolic complexes with NF-kappa B, trapping it in the cytoplasm. Complete folding of the region downstream of the GRR repeat precludes processing.
  Phosphorylation at 'Ser-903' and 'Ser-907' primes p105 for proteolytic processing in response to TNF-alpha stimulation. Phosphorylation at 'Ser-927' and 'Ser-932' are required for BTRC/BTRCP-mediated proteolysis.
  Polyubiquitination seems to allow p105 processing.
  S-nitrosylation of Cys-61 affects DNA binding.
• Cellular localizationNucleus. Cytoplasm. Nuclear, but also found in the cytoplasm in an inactive form complexed to an inhibitor.

Target information above from: UniProt accession P19838 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010) .

Information by UniProt
• Database links
  • Entrez Gene: 4790 Human
  • Omim: 164011 Human
  • SwissProt: P19838 Human
  • Unigene: 618430 Human

• Alternative names
  DKFZp686C01211 antibodyDNA binding factor KBF1 antibodyDNA binding factor KBF1 EBP1 antibody

  DNA-binding factor KBF1 antibodyEBP 1 antibodyEBP-1 antibodyEBP1 antibodyKBF1 antibodyMGC54151 antibodyNF kappa B antibodyNF kappabeta antibodyNF kB1 antibodyNFKB 1 antibodyNFKB p105 antibodyNFKB p50 antibodyNFKB1 antibodyNFKB1_HUMAN antibodyNuclear factor kappa B DNA binding subunit antibodyNuclear factor NF kappa B p105 subunit antibodyNuclear factor NF kappa B p50 subunit antibodyNuclear factor NF-kappa-B p50 subunit antibodyNuclear factor of kappa light polypeptide gene enhancer in B cells 1 antibodyNuclear factor of kappa light polypeptide gene enhancer in B-cells 1 antibodyp84/NF-kappa-B1 p98 antibody

  see all

Anti-NFkB p105 / p50 antibody images

• 

  Western blot - NFkB p105 / p50 antibody (ab75728)
  Anti-NFkB p105 / p50 antibody (ab75728) at 1/50 dilution + SK-BR-3 cell lysate at 35 µg
  
  Predicted band size : 105 kDa
  Observed band size : 105 kDa
  Additional bands at : 40 kDa. We are unsure as to the identity of these extra bands.