Recombinant Human Amyloid Precursor Protein Fc Chimera, CF Summary
| Additional Information |
Isoform APP695 |
| Details of Functionality |
Measured by its binding ability in a functional ELISA. When Recombinant Mouse Contactin-3
(Catalog #
9800-CN)
is coated at 2 µg/mL, 100 μL/well, Recombinant Human APP695 Fc Chimera
binds with an ED 50 of 7-42 ng/mL |
| Source |
Mouse myeloma cell line, NS0-derived human APP695 protein Human Amyloid-beta A4 (Isoform APP695) (Leu18-Lys612) Accession # P05067-4 | DIEGRMD | Human IgG1 (Pro100-Lys330) | | N-terminus | | C-terminus | |
|
| Accession # |
|
| N-terminal Sequence |
Leu18 |
| Structure / Form |
Disulfide-linked homodimer
|
| Protein/Peptide Type |
Recombinant Proteins |
| Purity |
>85%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Endotoxin Note |
<0.10 EU per 1 μg of the protein by the LAL method. |
Applications/Dilutions
| Dilutions |
|
| Theoretical MW |
94 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
| SDS-PAGE |
111-133 kDa, reducing conditions |
Packaging, Storage & Formulations
| Storage |
- 12 months from date of receipt, ≤ -20 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 3 months, ≤ -20 °C under sterile conditions after reconstitution.
|
| Buffer |
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. |
| Purity |
>85%, by SDS-PAGE visualized with Silver Staining and quantitative densitometry by Coomassie® Blue Staining |
| Reconstitution Instructions |
Reconstitute at 500 μg/mL in PBS. |
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Human Amyloid Precursor Protein Fc Chimera, CF
Background
Amyloid precursor protein (APP) is a type I
membrane protein with several isoforms due to alternative splicing. Of the
three major splice isoforms of APP (APP695, APP751, and APP770) APP695 is the
predominant neuronal form from which Amyloid beta peptide and transcriptionally-active cleaved
intracellular domain of APP (AICD) are preferentially generated by selective
processing through the amyloidogenic pathway (1). Human APP695 consists of a 17
amino acid (aa) signal sequence, a 607 aa extracellular domain (ECD), a 24 aa
transmembrane domain, and a 47 aa cytoplasmic domain. Within the ECD, human
APP695 shares 97% aa sequence identity with mouse and rat APP695. Amyloid beta is a major
molecule implicated in pathogenesis of Alzheimer's disease (AD) and related
dementias (2). AICD regulates expression by direct promoter binding of multiple
genes, including APP itself, the beta-secretase, BACE-1 and the Amyloid beta-degrading
enzyme, Neprilysin (3, 1). As such, APP695 plays an important role in brain
development, learning and memory, synaptic plasticity, and neurodegeneration
including AD (4).
- Nalivaeva, N.N. and Turner A. J. (2013) FEBS Lett. 587:2046.
- Haass, C. (2004) EMBO J. 23:483.
- Passer, B. et al. (2000) J. Alzheimers Dis. 2:289.
- Benilova, I. et al. (2012) Nat. Neurosci. 15:349.
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