Anti-Syntaxin 6抗体[3D10] - Golgi膜Marker
参阅全部 Syntaxin 6 一抗
小鼠单克隆抗体[3D10] to Syntaxin 6 - Golgi膜Marker
Mouse
适用于: Flow Cyt, WB, IPmore details
与反应: Mouse, Rat
Recombinant full length protein corresponding to Rat Syntaxin 6.
Database link: Q63635
The epitope for this antibody has been localized to the amino terminus (residues 1-25) of Syntaxin 6.
Mouse Brain Tissue Extract, rat Brain Tissue Extract.
This product was changed from ascites to tissue culture supernatant on 5th July 2019. Lot numbers higher than GR3173630 are from tissue culture supernatant. Please note that the dilutions may need to be adjusted accordingly. If you have any questions, please do not hesitate to contact our scientific support team.
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Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.09% Sodium azide
Constituents: PBS, 50% Glycerol (glycerin, glycerine)
浓度
100 µg 浓度为 1 mg/ml
Protein G purified
Purified from TCS
单克隆
3D10
IgG1
kappa
Abpromise™承诺保证使用ab12370于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度;实际最佳的稀释度/浓度应由使用者检定。
应用 | Ab评论 | 说明 |
---|---|---|
Flow Cyt | Use 2µg for 106 cells. ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody. | |
WB | (2) | 1/1000. Detects a band of approximately 35 kDa (predicted molecular weight: 30.6 kDa). |
IP | Use at an assay dependent concentration. |
Entrez Gene: 58244 Mouse
SwissProt: Q9JKK1 Mouse
Unigene: 465911 Mouse
Unigene: 66264 Mouse
Unigene: 100217 Rat
Laminin-1 subunit gamma antibody
Laminin-10 subunit gamma antibody
Laminin-11 subunit gamma antibody
STX 6 antibody
STX6 antibody
STX6_HUMAN antibody
Syntaxin-6 antibody
Syntaxin6 antibody
LAMB2 antibody
LAMC1 antibody
Laminin B2 chain antibody
Western blot - Anti-Syntaxin 6 antibody [3D10] - Golgi Membrane Marker (ab12370)
All lanes : Anti-Syntaxin 6 antibody [3D10] - Golgi Membrane Marker (ab12370) at 1 µg/ml
Lane 1 : Brain (Mouse) Tissue Lysate
Lane 2 : Brain (Rat) Tissue Lysate
Lysates/proteins at 10 µg per lane.
Secondary
All lanes : Goat Anti-Mouse IgG H&L (HRP) preadsorbed (ab97040) at 1/5000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 30.6 kDa
Observed band size: 30.6 kDa
Additional bands at: 26 kDa. We are unsure as to the identity of these extra bands.
Exposure time: 8 minutes
This image was generated using the ascites version of the product.
Western blot - Anti-Syntaxin 6 antibody [3D10] - Golgi Membrane Marker (ab12370)Image from Jonas MC et al, J Cell Sci. 2010 Oct 1;123(Pt 19):3378-88. Epub 2010 Sep 7, Fig 1, doi:10.1242/jcs.068841.
Intracellular membranes from CHO cells were separated on a 10–24% discontinuous Nycodenz gradient. Western Blotting was then performed using a range of antibodies including ab12370 at a 1/1000 dilution. An HRP-conjugated anti-mouse secondary was used at a 1/6000 dilution.
This image was generated using the ascites version of the product.
Immunoprecipitation - Anti-Syntaxin 6 antibody [3D10] - Golgi Membrane Marker (ab12370)
Syntaxin 6 was immunoprecipitated using 0.5mg Mouse Brain whole tissue lysate, 10µg of Mouse monoclonal to Syntaxin 6 and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, Mouse Brain whole tissue lysate lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab12370.
Secondary: Protein G-HRP at 1/500 dilution.
Band: 25kDa:Syntaxin 6.
This image was generated using the ascites version of the product.
Flow Cytometry - Anti-Syntaxin 6 antibody [3D10] - Golgi Membrane Marker (ab12370)
Overlay histogram showing PC12 cells stained with ab12370 (red line). The cells were fixed with 4% paraformaldehyde (10 min) 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 (ab12370, 2µg/1x106 cells) 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 image was generated using the ascites version of the product.