MAPKBP1-Polyclonal Antibodies

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MAPKBP1

Qty


Total
$220
Catalog #
A2626
Antibody Type
Polyclonal Antibody
Gene ID
23005
Swiss Prot
O60336
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC
Recommended DilutionWB 1:200 - 1:500 IHC 1:50 - 1:100
Calculated MW109kDa,164kDa
Observed MWRefer to Figures
ImmunogenA synthetic peptide of human MAPKBP1
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
SynonymJNKBP-1; MGC138851; MGC138852;
Images
  • A2626: image 1

    Western blot analysis of extracts of mouse liver tissue, using MAPKBP1 antibody.

  • A2626: image 2

    Immunohistochemistry of paraffin-embedded mouse stomach using MAPKBP1 antibody at dilution of 1:100 (x40 lens).

  • A2626: image 3

    Immunohistochemistry of paraffin-embedded human stomach using MAPKBP1 antibody at dilution of 1:100 (x40 lens).

Background

MAP kinases play a significant role in many biological processes, including cell adhesion and spreading, cell differentiation and apoptosis. MAPKBP-1 (mitogen-activated protein kinase binding protein 1), also known as JNKBP-1, is a 1,514 amino acid protein that contains twelve WD repeats. Induced by TRAF2 (TNF receptor-associated factor 2) and Tak1 (TGF-β-activated kinase 1), MAPKBP-1 is thought to act an adaptor protein for NFκB (nuclear factor κ-B) activation. MAPKBP-1 interacts with JNK3 and may promote TRAF2 polyubiquitination. MAPKBP-1 exists as six alternatively spliced variants and is encoded by a gene located on human chromosome 15. Human chromosome 15 houses over 700 genes and comprises nearly 3% of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.

Protocol

N/A

MSDS
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