Late-Onset Alzheimer's Disease Risk Gene (Mouse Model) Antibody Sampler Kit

The Late-Onset Alzheimer's Disease Risk Gene (Mouse Model) Antibody Sampler Kit provides an economical means of detecting proteins identified as risk factors for late-onset Alzheimer’s Disease (LOAD) by western blot. This kit includes enough antibodies to perform at least two western blot experiments with each primary antibody.

Alzheimer's Disease (AD) is the leading cause of dementia worldwide. Clinically, it is characterized by the presence of extracellular amyloid plaques and intracellular neurofibrillary tangles, which result in neuronal dysfunction and cell death (1). Genome-wide association studies (GWAS) have identified a cohort of risk genes associated with late-onset AD (LOAD), including, but not limited to, APOE, BIN1, SORL1, TREM2, EphA1, MEF2C, ABCA7, and PTK2B (2).
 
APOE has three allele variants; ApoE2, ApoE3, and ApoE4; with ApoE4 associated with an increased risk of AD. Evidence suggests that this risk occurs through promotion of amyloid-beta plaque aggregation (1). ApoE4 is also associated with impaired microglial response, lipid transport, synaptic integrity and plasticity, glucose metabolism, and cerebrovascular integrity (3). Mutations in BIN1, primarily involved in endocytosis and maintaining cytoskeletal integrity in the brain, are suggested to play a role in the aggravation of tau pathology (4,5). Increased levels of BIN1 have been seen in AD postmortem brain tissue (5). SORL1 expression is decreased in the brain of AD patients (6). Studies have demonstrated a role for SORL1 as a neuronal sorting receptor that binds amyloid precursor protein (APP) and regulates its trafficking and proteolytic processing, thus regulating β-amyloid (Aβ) peptide production (7). The triggering receptor expressed on myeloid cells 2 (TREM2) is an innate immune receptor that is expressed on the cell surface of microglia, macrophages, osteoclasts, and immature dendritic cells (8). Research studies using AD mouse models indicate that deficiency and haploinsufficiency of TREM2 can lead to increased Aβ accumulation due to dysfunctional microglia response (9). EphA1 is a member of the ephrin family of receptor tyrosine kinases responsible for regulating cell morphology and motility (10). In the central nervous system (CNS), EphA1 plays a role in synaptic plasticity and axon guidance (11). EphA1 is involved in inflammatory signaling pathways (12), which may mean it plays a role in regulation of neuroinflammatory processes in AD (13). ATP-binding cassette sub-family A member 7 (ABCA7) functions to regulate phospholipid and cholesterol homeostasis in the CNS (14,15). ABCA7 dysfunction may contribute directly to AD pathogenesis by accelerating Aβ production and/or altering microglia-dependent phagocytosis of Aβ (16-18). MEF2C is a member of the myocyte enhancer factor 2 (MEF2) family of transcription factors shown to play a role in learning and memory formation through regulation of synaptic plasticity (19). Studies have shown that MEF2C may play a role in age-related microglial activation through IFN-I associated MEF2C deregulation (20,21). MEF2C may also act as a modulator for APP proteolytic processing of Aβ (22,23). Protein tyrosine kinase, Pyk2, encoded by the PTK2B gene, is a non-receptor tyrosine kinase highly expressed in neurons with implications in synaptic plasticity (24,25). In mouse models, knockout of Pyk2 impairs hippocampal-dependent memory and long-term potentiation (24). Overexpression of Pyk2 has been shown to protect neurons against Aβ42-induced synaptotoxicity (26). Pyk2 may also act as a kinase for tau phosphorylation and has been implicated as a modulator of tau toxicity (27,28).