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Overview:
| Product Name | Rubicon Antibody | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Rabbit Anti-Human Rubicon Polyclonal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species Reactivity | Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Applications | WB, ICC/IF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Antibody Dilution | WB (1:1000), ICC/IF (1:100); optimal dilutions for assays should be determined by the user. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Host Species | Rabbit | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen Species | Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen | Synthetic peptide from the N-terminal of Human Rubicon | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Concentration | 1 mg/ml | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Conjugates |
Alkaline Phosphatase, APC, ATTO 390, ATTO 488, ATTO 565, ATTO 594, ATTO 633, ATTO 655, ATTO 680, ATTO 700, Biotin, FITC, HRP, PE/ATTO 594, PerCP, RPE, Streptavidin, Unconjugated
StreptavidinProperties:
Streptavidin Datasheet Biotin | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| R-PE (R-Phycoerythrin) | ||
Overview:
R-PE Datasheet | ![]() | Optical Properties: λex = 565 nm λem = 575 nm εmax = 2.0×106 Φf = 0.84 Brightness = 1.68 x 103 Laser = 488 to 561 nm Filter set = TRITC |
Properties
| Storage Buffer | PBS, 50% glycerol, 0.09% sodium azide |
| Storage Temperature | -20ºC |
| Shipping Temperature | Blue Ice or 4ºC |
| Purification | Peptide Affinity Purified |
| Clonality | Polyclonal |
| Specificity | Detects ~95 kDa. |
| Cite This Product | StressMarq Biosciences Cat# SPC-668, RRID: AB_2705519 |
| Certificate of Analysis | A 1:1000 dilution of SPC-668 was sufficient for detection of Rubicon in 15 µg of human Hela cell lysates by ECL immunoblot analysis using goat anti-rabbit IgG:HRP as the secondary antibody. |
Biological Description
| Alternative Names | Run domain Beclin-1-interacting and cysteine-rich domain-containing protein Antibody, KIAA0226 Antibody, Rubicon Antibody, Baron Antibody, RUBCN Antibody, Beclin-1 associated RUN domain containing protein Antibody |
| Research Areas | Cancer, Autophagy, Cardiovascular System, Cell Signaling, Heart, Metabolism, Metabolism processes |
| Cellular Localization | Early endosome, Late Endosome, Lysosome |
| Accession Number | NP_001139114.1 |
| Gene ID | 9711 |
| Swiss Prot | Q92622 |
Product Images
Western blot analysis of Human HeLa cell lysates showing detection of ~108 kDa Rubicon protein using Rabbit Anti-Rubicon Polyclonal Antibody (SPC-668). Lane 1: Molecular Weight Ladder (MW). Lane 2: HeLa cell lysates. Load: 15 µg. Block: 5% Skim Milk in 1X TBST. Primary Antibody: Rabbit Anti-Rubicon Polyclonal Antibody (SPC-668) at 1:1000 for 2 hours at RT. Secondary Antibody: Goat Anti-Rabbit IgG: HRP at 1:1000 for 60 min at RT. Color Development: ECL solution for 6 min in RT. Predicted/Observed Size: ~108 kDa.
Immunocytochemistry/Immunofluorescence analysis using Rabbit Anti-Rubicon Polyclonal Antibody (SPC-668). Tissue: Colon carcinoma cell line (RKO). Species: Human. Fixation: 4% Formaldehyde for 15 min at RT. Primary Antibody: Rabbit Anti-Rubicon Polyclonal Antibody (SPC-668) at 1:100 for 60 min at RT. Secondary Antibody: Goat Anti-Rabbit ATTO 488 at 1:100 for 60 min at RT. Counterstain: Phalloidin Texas Red F-Actin stain; DAPI (blue) nuclear stain at 1:1000, 1:5000 for 60 min at RT, 5 min at RT. Localization: Late Endosome, Lysosome, Early Endosome . Magnification: 60X. (A) DAPI nuclear stain. (B) Phalloidin Texas Red F-Actin stain. (C) Rubicon Antibody. (D) Composite.
Product Citations (0)
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| ATTO 594 | ||
Overview:
ATTO 594 Datasheet | ![]() | Optical Properties: λex = 601 nm λem = 627 nm εmax = 1.2×105 Φf = 0.85 τfl = 3.5 ns Brightness = 102 Laser = 594 nm Filter set = Texas Red® |
StressMarq硫黄素T测定硫黄素T是一种荧光染料,可与富含β片层的结构(例如α突触核蛋白原纤维中的结构)结合。结合后,染料的发射光谱发生红移并增加了荧光强度。以下方案用于使用α突触核蛋白预制的原纤维和单体生成硫黄素T测定法。准备dH2O中的1mM硫黄素T储备溶液(新鲜制备,并通过0.2μm注射器过滤器过滤)。在PBS pH 7.4中稀释硫黄素T,使每孔中硫黄素T的最终浓度为25μM(每孔体积= 100μL)。板:Lumox 96多孔板(Sarstedt目录号94.6000.024)。使用前在室温下解冻α-突触核蛋白等分试样。将10μM预制纤维或100μM单体(或两者)添加到适当的孔中。用移液器上下吸取混合液。浓度是估算值,需要进行优化以给出良好的信号而不会造成浪费。密封板并置于37°C的振荡培养箱(600 rpm)中。使用Softmax Pro软件6.5.1版在Molecular Devices Gemini XPS微孔板读取器上测量荧光。 XPS微孔板读取器设置:温度:37°C读取类型:阱扫描波长:450 nm处的激发和485 nmPMT 处的发射增益:每次读取自动闪烁:6次摇动:读取前20秒7.重新密封板并放入37°C的振荡培养箱中。8.定期从1到72小时获取读数。
















