Anti-SNAP23 抗体
Anti-SNAP23 antibody
4
(7 Reviews)
|
(21 Publications)
Rabbit Polyclonal SNAP23 antibody. Suitable for IP, WB, IHC-P, ICC/IF and reacts with Recombinant fragment, Mouse, Rat, Human, Recombinant full length protein - Human samples. Cited in 21 publications. Immunogen corresponding to Synthetic Peptide within Mouse Snap23 aa 150 to C-terminus.
別名を表示する
Sndt, Synaptosomal-associated protein 23, SNAP-23, Syndet, Vesicle-membrane fusion protein SNAP-23
- ICC/IF
Supplier Data
Immunocytochemistry/ Immunofluorescence - Anti-SNAP23 antibody (AB3340)
Immunofluorescence analysis of SNAP-23 was performed using 90% confluent log phase U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) cells with ab3340. The cells were fixed with 4% paraformaldehyde for 10 minutes, permeabilized with 0.1% Triton™ X-100 for 10 minutes, and blocked with 1% BSA for 1 hour at room temperature. The cells were labeled with ab3340 at 2μg/mL in 0.1% BSA and incubated for 3 hours at room temperature and then labeled with Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, Alexa Fluor® 488 conjugate at a dilution of 1 : 2000 for 45 minutes at room temperature (Panel a : green). Nuclei (Panel b : blue) were stained with DAPI. F-actin (Panel c : red) was stained with Alexa Fluor® 555 Rhodamine Phalloidin (Product # R415, 1 : 300). Panel d represents the merged image showing membrane localization. Panel e shows the no primary antibody control. The images were captured at 60X magnification.
- IHC-P
Lab
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SNAP23 antibody (AB3340)
ab3340 (1ug/ml) staining SNAP23 in human tonsil using an automated system (DAKO Autostainer Plus). Using this protocol there is strong staining of cellular membrane compartments of the lymphatic nodules.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako envision flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
- ICC/IF
Unknown
Immunocytochemistry/ Immunofluorescence - Anti-SNAP23 antibody (AB3340)
ICC/IF image of ab3340 stained PC-12 (Rat adrenal gland pheochromocytoma cell line) cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab3340, 5μg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43μM.
- WB
Supplier Data
Western blot - Anti-SNAP23 antibody (AB3340)
Decrease in signal upon siRNA mediated knock down confirms that antibody is specific to SNAP23.
All lanes:
Western blot - Anti-SNAP23 antibody (ab3340) at 1 µg/mL
Lane 1:
Untransfected U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysates
Lane 2:
Non-specific scrambled siRNA transfected U-87 MG whole cell lysates
Lane 3:
SNAP23 KO U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysates
Secondary
All lanes:
Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate at 0.25 µg/mL
Predicted band size: 23 kDa
false
- WB
Supplier Data
Western blot - Anti-SNAP23 antibody (AB3340)
All lanes:
Western blot - Anti-SNAP23 antibody (ab3340) at 2 µg/mL
Lane 1:
U-87 MG (Human glioblastoma-astrocytoma epithelial cell line) whole cell lysate at 30 µg/mL
Lane 2:
HepG2 (Human liver hepatocellular carcinoma cell line) whole cell lysate at 30 µg/mL
Secondary
All lanes:
Goat anti-Rabbit IgG (H+L) Superclonal™ Secondary Antibody, HRP conjugate at 0.4 µg/mL
Predicted band size: 23 kDa
false
- WB
Unknown
Western blot - Anti-SNAP23 antibody (AB3340)
All lanes:
Western blot - Anti-SNAP23 antibody (ab3340)
All lanes:
Rat brain tissue
Predicted band size: 23 kDa
false
- WB
Unknown
Western blot - Anti-SNAP23 antibody (AB3340)
All lanes:
Western blot - Anti-SNAP23 antibody (ab3340) at 1 µg/mL
All lanes:
Western blot - Recombinant Human SNAP23 protein (<a href='/products/proteins-peptides/recombinant-human-snap23-protein-ab79180'>ab79180</a>) at 0.001 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) preadsorbed (<a href='/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-preadsorbed-ab97080'>ab97080</a>) at 1/5000 dilution
Predicted band size: 23 kDa
true
Exposure time: 2min
Reactivity data
出荷温度及び保存条件
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バッファー組成
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
保管に関する情報
補足情報
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SNAP23 plays a significant role in the regulation of membrane fusion events and intracellular transport. It forms part of the SNARE complex which includes v-SNAREs on vesicle membranes and other t-SNAREs on target membranes. This complex orchestrates the docking and fusion of vesicles enabling the release of neurotransmitters and other cargoes in neuronal and non-neuronal cells. By mediating these events SNAP23 is important for neurotransmission insulin-regulated glucose uptake and other cellular processes.
Pathways
SNAP23 functions in the exocytotic and endocytic pathways where it aids in the accurate secretion and recycling of cellular components. It interacts with proteins like Syntaxin and VAMP (vesicle-associated membrane protein) to achieve precise vesicle targeting and fusion. SNAP23 is also implicated in insulin-signaling pathways where it modulates GLUT4 translocation to the cell surface a process vital for maintaining glucose homeostasis. These interactions underline its involvement in both neural communication and metabolic regulation.
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文献 (21)
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Nature communications 15:2856 PubMed38565851
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Virology 578:117-127 PubMed36527930
2022
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Biological & pharmaceutical bulletin 45:1572-1580 PubMed36184518
2022
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eLife 10: PubMed33973520
2021
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The Journal of biological chemistry 296:100268 PubMed33837726
2021
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The Journal of biological chemistry 295:15045-15053 PubMed32848017
2020
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Nature communications 11:181 PubMed31924761
2020
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International journal of molecular sciences 20: PubMed30871020
2019
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Science signaling 12: PubMed30783011
2019
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Cancer letters 434:144-151 PubMed30036609
2018
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