Autophagosome markers are molecular tools used to identify, localize autophagosomes and evaluate autophagic activity, serving as core components in studying autophagic mechanisms and analyzing autophagic abnormalities related to diseases.

ATP-dependent chromatin remodeling complexes play an essential role in the regulation of various nuclear processes, such as gene expression, DNA replication, and repair. The SWI/SNF chromatin remodeling complex consists of more than 10 subunits with a single molecule of the ATPase catalytic subunit BRM or BRG1, but not both. The activities of these two subunits drive the disruption of histone-DNA contacts that lead to changes in accessibility of crucial regulatory elements within chromatin.

Autophagy vesicle elongation is a crucial phase in the autophagy process, during which Atg12 conjugation plays a vital role. In this process, Atg12 is covalently attached to Atg5 through a ubiquitin-like conjugation system to form the Atg12-Atg5 complex.

Aurora kinases belong to a highly conserved family of mitotic serine/threonine kinases with three members identified among mammals: Aurora A, B, and C. Studies on the temporal expression pattern and subcellular localization of Aurora kinases in mitotic cells suggest an association with mitotic structure.

α-thalassemia/mental retardation X-linked (ATRX) is a transcriptional regulator and helicase that belongs to the SNF2 family of chromatin remodeling proteins. Together with its binding partner death-associated protein 6 (Daxx), ATRX acts as histone chaperone to deposit histone variant H3.3 at repetitive DNA sequences such as telomeric, pericentric, and ribosomal gene repeats.

Autophagy Vesicle Elongation is a crucial phase in the autophagy process, primarily involving the conjugation of LC3 protein (LC3 Conjugation) and the expansion and closure of the autophagosome membrane.

Autophagy is a self-degradative process that is important for balancing sources of energy at critical times in development and in response to nutrient stress.

Astrocytes are the most prevalent type of glial cell in the CNS and are found within the brain and spinal cord. In a healthy nervous system, astrocytes play essential roles in development, regulation of blood flow (by supporting endothelial cells in the blood brain barrier), synaptic transmission and function, and energy and metabolism (by providing nutrients to neurons and synthesizing certain neurotransmitters). The loss or abnormal function of astrocytes is implicated in a wide variety of neurodegenerative disease processes. Chronic activation of astrocytes results in the formation of lesions similar to those observed in Alzheimer’s Disease and Huntington’s Disease. Some useful astrocyte markers include GFAP and ALDH1L1.

Low density lipoprotein receptor related protein 1 (LRP1) is a type I transmembrane receptor that mediates the endocytosis of various ligands, including apolipoproteins and tau. Both proteins are genetically and pathologically linked to Alzheimer's disease (AD).Postsynaptic Density protein 95 (PSD95) is a member of the membrane-associated guanylate kinase (MAGUK) family of proteins that functions as a scaffolding protein to promote assembly and function of the postsynaptic density complex .

Apoptosis is a strictly regulated process that leads to orderly cell breakdown and clearance. Unlike necrotic cell death, apoptosis is well regulated and plays a critical role in development, immune function, and tissue homeostasis. Normal cells undergo apoptosis when subjected to various endogenous and exogenous stimuli to maintain a balance between cell survival and death.