Rabbit Recombinant Monoclonal ZFY26 antibody. Suitable for WB and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
WB | IHC-P | IHC-Fr | ICC/IF | |
---|---|---|---|---|
Human | Tested | Not recommended | Not recommended | Not recommended |
Mouse | Tested | Not recommended | Not recommended | Not recommended |
Rat | Tested | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000 | Notes - |
Species Mouse | Dilution info 1/1000 | Notes - |
Species Rat | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human, Rat | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human, Mouse, Rat | Dilution info - | Notes - |
Phosphatidylinositol 3-phosphate-binding protein required for the abscission step in cytokinesis: recruited to the midbody during cytokinesis and acts as a regulator of abscission. May also be required for efficient homologous recombination DNA double-strand break repair.
KIAA0321, ZFYVE26, Zinc finger FYVE domain-containing protein 26, FYVE domain-containing centrosomal protein, Spastizin, FYVE-CENT
Rabbit Recombinant Monoclonal ZFY26 antibody. Suitable for WB and reacts with Human, Mouse, Rat samples.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 59% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
ZFYVE26 also known as spastizin is a protein with a mass of approximately 260 kDa. It functions as a zinc finger FYVE-type containing protein which participates in intracellular trafficking and endosomal transport. ZFYVE26 locates in the cytoplasm and its expression appears in many tissues but it is particularly abundant in the nervous system where it suggests an important cellular role. Through its FYVE domain it directly binds to phosphatidylinositol 3-phosphate (PtdIns3P) on endosomal membranes a feature that defines its mechanical operation.
ZFYVE26 regulates endosome-to-trans-Golgi network trafficking and may also facilitate autophagic processes. It forms part of a protein complex involved in shaping the tubular endosomal networks working alongside other proteins like spatacsin. This association aids in maintaining cellular homeostasis by preventing the accumulation of dysfunctional endosomes. ZFYVE26 also influences the stability and positioning of the cytoskeleton by interacting with specific cytoskeletal components.
ZFYVE26 plays roles in autophagy and endocytosis pathways. It associates with proteins such as spatacsin and atlastin-1 in these pathways which together modulate membrane dynamics. In autophagy ZFYVE26 ensures the maturation of autophagosomes while in endocytosis it facilitates the recycling of membrane constituents. These interactions ensure proper intracellular communication and material recycling important for cellular regular function.
Defects in ZFYVE26 cause hereditary spastic paraplegia (HSP) a disorder marked by spasticity and weakness of lower limbs. Mutations disrupt its function affecting endosomal pathway and axonal transport leading to neurodegeneration. It's closely associated with proteins like spatacsin in these pathological processes. Additionally ZFYVE26 has connections to amyotrophic lateral sclerosis (ALS) where defective endosomal systems and protein aggregation contribute to motor neuron degeneration and disease progression.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
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.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 24367272).
The identity of the bands beneath 285 kDa are unknown.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
All lanes: Western blot - Anti-ZFYVE26 antibody [EPR28782-59] (ab319051) at 1/1000 dilution
Lane 1: HeLa (human cervical adenocarcinoma epithelial cell) transfected with scrambled siRNA control whole cell lysate at 20 µg
Lane 2: HeLa transfected with siRNA specifically targeting ZFYVE26 whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 285 kDa, 36 kDa
Exposure time: 92s
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 24367272).
The identity of the bands beneath 285 kDa are unknown.
Exposure time: Lanes 1-4: 92 seconds; Lanes 5-6: 180 seconds.
All lanes: Western blot - Anti-ZFYVE26 antibody [EPR28782-59] (ab319051) at 1/1000 dilution
Lane 1: SK-MEL-2 (human skin malignant melanoma cell) whole cell lysate at 20 µg
Lane 2: SH-SY5Y (human neuroblastoma epithelial cell) whole cell lysate at 20 µg
Lane 3: HEK-293 (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Lane 4: NIH/3T3 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 5: 3T3-L1 (mouse embryonic fibroblast) whole cell lysate at 20 µg
Lane 6: PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 285 kDa
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Low expression: skeletal muscle, heart (PMID: 24367272).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID: 24367272).
Lanes 1-2 are applied with Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG (Merck DC03L) at 1/2000 and lanes 3-9 are applied with Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000
The identity of the bands beneath 285 kDa in lane 1, 3 and lane 9 are unknown.
In Western blot, Anti-GAPDH antibody [EPR16891] - Loading Control (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) staining at 1/200000 dilution.
All lanes: Western blot - Anti-ZFYVE26 antibody [EPR28782-59] (ab319051) at 1/1000 dilution
Lane 1: Human cerebellum tissue lysate at 20 µg
Lane 2: Human skeletal muscle tissue lysate at 20 µg
Lane 3: Mouse liver tissue lysate at 20 µg
Lane 4: Mouse brain tissue lysate at 20 µg
Lane 5: Mouse skeletal muscle tissue at 20 µg
Lane 6: Mouse heart tissue lysate at 20 µg
Lane 7: Rat liver tissue lysate at 20 µg
Lane 8: Rat skeletal muscle tissue at 20 µg
Lane 9: Rat heart tissue lysate at 20 µg
Lanes 1 - 2: Goat Anti-Rabbit IgG (HRP) with minimal cross-reactivity with human IgG at 1/2000 dilution
Lanes 3 - 9: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/20000 dilution
Observed band size: 285 kDa, 36 kDa
Exposure time: 92s
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