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Read our guarantee »Anti-ITM2B antibody
See all ITM2B products (8) ...
Chicken polyclonal to ITM2B
WB, IHC-Pmore details
Reacts with
Mouse, Rat, Human
Synthetic peptide: MVKVTFNSAL AQKEAKKDEP KSGEEALIIP PDAVAVDCKD PDDVVPVGQR RAWCWCMCFG, corresponding to amino acids 1-60 of ITM2B.
MVKVTFNSAL AQKEAKKDEP KSGEEALIIP PDAVAVD CKD PDDVVPVGQR RAWCWCMCFG
E Coli-derived fusion protein.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: None
Constituents: PBS
Concentration information loading...
Immunogen affinity purified
Polyclonal
IgY
Neuroscience >> Neurology process >> Neurogenesis
Neuroscience >> Neurology process >> Neurodegenerative disease >> Other
Neuroscience >> Sensory System >> Auditory system
Western blot - ITM2B antibody (ab14307)
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Our Abpromise guarantee covers the use of ab14307 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/2000. Predicted molecular weight: 32 kDa.
IHC-P: Use at an assay dependent dilution. See Abreview.
Functions as a protease inhibitor. Plays a role in APP processing regulating the physiological production of the beta amyloid peptide. Restricts docking of gamma-secretase to APP and access of alpha- and beta-secretase to their cleavage APP sequence.
Expressed in brain and in other tissues.
Defects in ITM2B are a cause of cerebral amyloid angiopathy ITM2B-related type 1 (CAA-ITM2B1) [MIM:176500]. A disorder characterized by amyloid deposition in the walls of cerebral blood vessels and neurodegeneration in the central nervous system. Cerebral amyloid angiopathy, non-neuritic and perivascular plaques and neurofibrillary tangles are the predominant pathological lesions. Clinical features include progressive mental deterioration, spasticity and muscular rigidity.
Defects in ITM2B are a cause of cerebral amyloid angiopathy ITM2B-related type 2 (CAA-ITM2B2) [MIM:117300]; also known as heredopathia ophthalmo-oto-encephalica. A disorder characterized by amyloid deposition in the walls of the blood vessels of the cerebrum, choroid plexus, cerebellum, spinal cord and retina. Plaques and neurofibrillary tangles are observed in the hippocampus. Clinical features include progressive ataxia, dementia, cataracts and deafness.
Belongs to the ITM2 family.
Contains 1 BRICHOS domain.
The C-terminal part of the ectodomain is processed by furin and related proteases producing a secreted peptide of 4 to 5 kDa. For the ABRI and ADAN variants the C-terminal secreted peptide is larger and may produce amyloid fibrils responsible for neuronal dysfunction and dementia. The remaining part of the ectodomain containing the BRICHOS domain is cleaved by ADAM10 and is secreted as a peptide of 25 kDa. The membrane-bound N-terminal fragment (NTF) of 22 kDa is further proteolytically processed by SPPL2A and SPPL2B through regulated intramembrane proteolysis producing a secreted peptide (BRI2C) and an intracellular domain (ICD) released in the cytosol.
Golgi apparatus membrane. Cell membrane.
Target information above from: UniProt accessionQ9Y287
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - ITM2B antibody (ab14307)

Anti-ITM2B antibody (ab14307) at 1/2000 dilution + E.coli derived ITM2B fusion protein
Secondary
HRP conjugated goat anti IgY at 1/1000 dilution
Predicted band size : 32 kDa
This product has been referenced in:
See all 4 publications for this product
Publishing research using ab14307? Please let us know so that we can cite the reference in this datasheet
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