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Read our guarantee »Products:Signal Transduction >> Protein Trafficking >> Vesicle Transport >> SNAPs & SNAREs
Anti-SYBL1 antibody [158.2]
See all SYBL1 products (6) ...
Mouse monoclonal [158.2] to SYBL1
Flow Cyt, ICC/IF, WB, IHC-Fr, IHC-Pmore details
Reacts with
Rat, Human
Predicted to work with
Mouse, Dog
Recombinant full SYBL1 protein (Human)
extract from rat brain
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze / thaw cycles.
Preservative: None
Constituents: Ascites
Concentration information loading...
Ascites
Monoclonal
158.2
IgG1
kappa
Signal Transduction >> Protein Trafficking >> Vesicle Transport >> Regulation
Signal Transduction >> Protein Trafficking >> Vesicle Transport >> SNAPs & SNAREs
Our Abpromise guarantee covers the use of ab36195 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Flow Cyt: 1/50
ICC/IF: Use at an assay dependent dilution. (PubMed: 19138172)
WB: 1/500 - 1/2000.Predicted molecular weight: 24 kDa.
IHC-Fr: 1/10 - 1/400.
IHC-P: 1/10 - 1/400.
Involved in the targeting and/or fusion of transport vesicles to their target membrane during transport of proteins from the early endosome to the lysosome. Required for heterotypic fusion of late endosomes with lysosomes and homotypic lysosomal fusion. Required for calcium regulated lysosomal exocytosis. Involved in the export of chylomicrons from the endoplasmic reticulum to the cis Golgi. Required for exocytosis of mediators during eosinophil and neutrophil degranulation, and target cell killing by natural killer cells. Required for focal exocytosis of late endocytic vesicles during phagosome formation.
Detected in all tissues tested.
Belongs to the synaptobrevin family.
Contains 1 longin domain.
Contains 1 v-SNARE coiled-coil homology domain.
Cytoplasmic vesicle > secretory vesicle membrane. Golgi apparatus > trans-Golgi network membrane. Late endosome membrane. Lysosome membrane. Endoplasmic reticulum membrane. Cytoplasmic vesicle > phagosome membrane.
Target information above from: UniProt accessionP51809
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - SYBL1 antibody [158.2] (ab36195)
![Western blot - SYBL1 antibody [158.2] (ab36195)](/ps/datasheet/images/36/ab36195/SYBL1-Primary-antibodies-ab36195-1.jpg)
Anti-SYBL1 antibody [158.2] (ab36195) at 1/500 dilution + Tissue lysates prepared from rat brain
Predicted band size : 24 kDa
Flow Cytometry-SYBL1 antibody [158.2](ab36195)
](/ps/datasheet/images/36/ab36195/SYBL1-Primary-antibodies-ab36195-3.jpg)
Overlay histogram showing PC12 cells stained with ab36195 (red line). The cells were fixed with 4% paraformaldehyde and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab36195, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (ab96879) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG1 [ICIGG1] (ab91353, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in PC12 cells fixed with methanol (5 min)/permeabilized with 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 7 publications for this product
Publishing research using ab36195? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
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![Western blot - SYBL1 antibody [158.2] (ab36195)](/ps/datasheet/images/36/ab36195/SYBL1-Primary-antibodies-ab36195-1.jpg)
Anti-SYBL1 antibody [158.2] (ab36195) at 1/500 dilution + Tissue lysates prepared from rat brain
Predicted band size : 24 kDa
](/ps/datasheet/images/36/ab36195/SYBL1-Primary-antibodies-ab36195-3.jpg)
Overlay histogram showing PC12 cells stained with ab36195 (red line). The cells were fixed with 4% paraformaldehyde and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab36195, 1/50 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-mouse IgG (H+L) (
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