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- 文献和实验
- 技术资料
- 应用范围:
Immunoprecipitation;Western Blotting
- 宿主:
Mouse
- 抗原来源:
0
- 适应物种:
Bovine;Human;Mouse;Rat
- 库存:
大量
- 是否单克隆:
1
- 规格:
200 μg
Product Images
WB: A431 (lane 1) and NIH 3T3 (lane 2) cell lysates probed with anti-PP2A.
Western Blot Analysis:
Representative image from a previous lot.
A431 (lane 1) and 3T3 (lane 2) cell lysates were resolved by electrophoresi...
| Species Reactivity | Key Applications | Host | Format | Antibody Type |
|---|---|---|---|---|
| H, R, M, B, Rb, Xn, Yeast (S. cerevisiae ) | IC, IP, WB | Mouse | Purified | Monoclonal Antibody |
- Replication protein C
- protein phosphatase 2 (formerly 2A), catalytic subunit, alpha isoform
- protein phosphatase 2, catalytic subunit, alpha isoform
- serine/threonine protein phosphatase 2A, catalytic subunit, alpha isoform
- Immunocytochemistry
- Immunoprecipitation
- Western Blotting
4 µg of a previous lot immunoprecipitated PP2A from 500 µg of A431 RIPA lysate. Note: This antibody has been reported not to block phosphatase activity.
Immunocytochemistry:
5-10 µg/mL of a previous lot of this antibody showed positive immunostaining for PP2A in A431 cells fixed for 10 minutes with 4% paraformaldehyde in PBS.
- Human
- Rat
- Mouse
- Bovine
- Rabbit
- Xenopus
- Yeast (S. cerevisiae )
Included Positive Antigen Control: Catalog # 12-301, non stimulated A431 lysate. Add 2.5 μL of 2-mercaptoethanol per 100 μL of lysate and boil for 5 minutes to reduce the preparation. Load 20 μg of reduced lysate per lane for minigels.
- PPP2CA
- PP2CA
- PP2A-alpha
- PP2Ac
- RP-C
Western Blot Analysis:
0.5-2 µg/mL of this lot detected PP2A in human A431 and previously in murine 3T3 RIPA cell lysates.
- Signaling
- Neuroscience
- Neurotransmitters & Receptors
- Neurodegenerative Diseases
更多产品技术资讯,请访问密理博中国博客:http://blog.milliporechina.com
peptide (C-RGEPHVTRRTPDYFL) corresponding to amino acids 295-309 of the 36kDa catalytic subunit of human protein phosphatase 2A (PP2A) 详细描述见链接:http://www.millipore.com/catalogue/item/05-421
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文献和实验Dual- and Triple-Color Fluorospot
stimulatory agents of choice and anti-CD28 (0.1 μg/ml; seeNote 4), in a final volume of 100–150 μl/well. The number of cells per well is dependent on the stimulating agent used (seeNote 5). b. Incubate the plate overnight at 37°C in a humidified
Immunodetection of cyclin D1 and D2/D3 using flow cytometry
that has been kept -20°C. Incubate the cells for at least two hours. Wash once with staining buffer and decant. Add the primary anti-cyclin antibody in a volume of 200 µ l. Incubate overnight at 4°C. Wash twice with cold cyclin staining buffer and add the Cy
13342), LDL-DiI (L3482), cholera toxin subunit B-Alexa 647 (C34778), dextran-Alexa 488 (D22910) and dextran-Alexa 594 (D22913) Protease inhibitors: leupeptin hemisulfate (AppliChem, cat. no. A2183), aprotinin (AppliChem, cat. no. A2132
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