Rabbit Polyclonal ATG9B antibody. Suitable for WB, ICC/IF and reacts with Rat, Human samples. Immunogen corresponding to Synthetic Peptide within Human ATG9B aa 100-150.
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
WB | ICC/IF | |
---|---|---|
Human | Expected | Tested |
Mouse | Predicted | Predicted |
Rat | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
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Phospholipid scramblase involved in autophagy by mediating autophagosomal membrane expansion. Cycles between the preautophagosomal structure/phagophore assembly site (PAS) and the cytoplasmic vesicle pool and supplies membrane for the growing autophagosome. Lipid scramblase activity plays a key role in preautophagosomal structure/phagophore assembly by distributing the phospholipids that arrive through ATG2 (ATG2A or ATG2B) from the cytoplasmic to the luminal leaflet of the bilayer, thereby driving autophagosomal membrane expansion (By similarity). In addition to autophagy, also plays a role in necrotic cell death (By similarity).
APG9L2, NOS3AS, ATG9B, Autophagy-related protein 9B, APG9-like 2, Nitric oxide synthase 3-overlapping antisense gene protein, Protein sONE
Rabbit Polyclonal ATG9B antibody. Suitable for WB, ICC/IF and reacts with Rat, Human samples. Immunogen corresponding to Synthetic Peptide within Human ATG9B aa 100-150.
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
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ATG9B also known as APG9L2 plays a central role in autophagy. This protein has an approximate mass of 106 kDa and is primarily expressed in the human brain and heart with lower levels found in other tissues. Functionally ATG9B interacts with cellular membranes and is involved in trafficking between organelles helping to form autophagosomes. While studying its mechanisms researchers have found its expression patterns closely link to the areas where metabolic regulation is critical.
Proteins like ATG9B facilitate cellular homeostasis by modulating autophagic response activities. ATG9B is a core component of the autophagy machinery; it localizes to the trans-Golgi network and endosomes playing a regulatory function in the early stages of autophagosome formation. As part of the larger ATG protein complex it ensures proper vesicle nucleation and elongation required for autophagosome maturation. This involvement highlights its pivotal role in maintaining cellular health especially under stressful conditions.
ATG9B is significant in the macroautophagy and mTOR signaling pathways. ATG9B functions closely with ATG7 and ATG12 which are essential for autophagosome efficiency in the macroautophagy pathway. The mTOR pathway which regulates cell growth and metabolism responding to nutrients energy and stress can influence ATG9B actions. This interconnectedness explains how cells adjust their metabolic throughput under conditions like nutrient scarcity or hypoxic stress highlighting the complexity of these cellular survival mechanisms.
Scientists have linked ATG9B to neurodegenerative diseases and cancer. Impaired autophagic roles or dysfunctional regulation associated with ATG9B can lead to conditions like Huntington's disease where protein aggregates accumulate due to insufficient degradation. In cancer ATG9B's role diverges where it may either suppress or support tumorigenesis depending on the cellular context. The relationship with proteins such as p53 in cancer emphasizes how ATG9B potentially influences cell death and survival pathways making it of interest for therapeutic studies.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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Immunofluorescent analysis of 4% paraformaldehyde-fixed SK-N-BE (human neuroblastoma cell line) cells labeling ATG9B with ab240897 at 1/100 dilution for 60 minutes at room temperature, followed by Goat Anti-Rabbit ATTO 488 at 1/200 dilution for 60 minutes (green). The nuclear counter stain is DAPI (blue). Actin is detected with Phalloidin Texas Red F-Actin stain (red).
A: DAPI, B: Actin, C: ATG9B, D: Composite.
Primary incubation for 16 hours at 4°C.
All lanes: Western blot - Anti-ATG9B antibody (ab240897) at 1/1000 dilution
All lanes: Rat brain lysate at 15 µg
All lanes: Goat Anti-Rabbit IgG: HRP at 1/2000 dilution
Developed using the ECL technique.
Predicted band size: 101 kDa
Exposure time: 6min
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