Anti-PABP抗体[10E10] (ab6125)
Key features and details
- Mouse monoclonal [10E10] to PABP
- Suitable for: WB, IP, Flow Cyt
- Reacts with: Rabbit, Chicken, Human, Xenopus laevis
- Isotype: IgG2b
概述
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产品名称
Anti-PABP抗体[10E10]
参阅全部 PABP 一抗 -
描述
小鼠单克隆抗体[10E10] to PABP -
宿主
Mouse -
经测试应用
适用于: WB, IP, Flow Cytmore details -
种属反应性
与反应: Rabbit, Chicken, Human, Xenopus laevis
不与反应: Mouse, Drosophila melanogaster -
免疫原
Recombinant PABP (Human) expressed from its 1.85 kbp cDNA, NcoI to SspI.
性能
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形式
Liquid -
存放说明
Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle. -
存储溶液
Preservative: 0.1% Sodium azide
Constituent: PBS -
Concentration information loading... -
纯度
Protein A purified -
纯化说明
Purified from supernatant. -
克隆
单克隆 -
克隆编号
10E10 -
骨髓瘤
Sp2/0 -
同种型
IgG2b -
研究领域
相关产品
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Compatible Secondaries
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Conjugation kits
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Isotype control
应用
Our Abpromise guarantee covers the use of ab6125 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
| 应用 | Ab评论 | 说明 |
|---|---|---|
| WB | Use at an assay dependent concentration. Detects a band of approximately 70 kDa (predicted molecular weight: 71 kDa). | |
| IP | Use at an assay dependent concentration. | |
| Flow Cyt | Use 1µg for 106 cells. ab170192 - Mouse monoclonal IgG2b, is suitable for use as an isotype control with this antibody.
|
靶标
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相关性
The poly(A)-binding protein (PABP), which is found complexed to the 3-prime poly(A) tail of eukaryotic mRNA, is required for poly(A) shortening and translation initiation. Grange et al. (1987) isolated a melanoma cell cDNA encoding human PABP. The predicted 633-amino acid protein contains 4 repeats of an approximately 80-amino acid unit in its N-terminal half. The authors found that this repeat region is highly conserved between human and yeast PABP and is sufficient for poly(A) binding. In vitro translation of the human PABP cDNA yielded a protein with an apparent molecular mass of 73 kD by SDS-PAGE. Northern blot analysis indicated that PABP is expressed as a 2.9-kb mRNA in human melanoma cells. Gorlach et al. (1994) noted that each of the 4 repeats of PABP is a ribonucleoprotein (RNP) consensus sequence RNA-binding domain. They determined that PABP has a pI of approximately 10.3 and is a very abundant, stable protein. Immunofluorescence studies of mammalian cells indicated that PABP is located exclusively in the cytoplasm. However, using both indirect immunofluorescence and tagging of PABP1 by fusion to the green fluorescent protein (GFP), Afonina et al. (1998) demonstrated that PABP1 shuttles between the nucleus and cytoplasm. PABP1 accumulated in the nucleus when transcription was inhibited, suggesting that active transcription is required for nuclear export of PABP1. -
细胞定位
Cytoplasmic. Shuttles between the cytoplasm and the nucleus. -
数据库链接
- Entrez Gene: 26986 Human
- Omim: 604679 Human
- SwissProt: P11940 Human
- Unigene: 387804 Human
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别名
- PAB 1 antibody
- PAB1 antibody
- PABP 1 antibody
see all
图片
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![Western blot - Anti-PABP antibody [10E10] (ab6125)](https://www.abcam.cn/ps/products/6/ab6125/Images/ab6125-12039-anti-pabp-antibody-10e10-western-blot.jpg)
Western blot - Anti-PABP antibody [10E10] (ab6125)This image is courtesy of an abreview submitted by Francisco Ramirez-ValleAll lanes : Anti-PABP antibody [10E10] (ab6125) at 1/2000 dilution
Lane 1 : 10ug of protein from MCF10A cells transfected with negative control siRNA.
Lane 2 : 10ug of protein from MCF10A cells transfected with PABP specific siRNA.
Lane 3 : 10 ug of protein from MCF10A cells transfected with PABP specific siRNA.
Secondary
All lanes : Goat anti-mouse 1/10000
Predicted band size: 71 kDa
Observed band size: 70 kDa why is the actual band size different from the predicted?
The cells were lysed with NP40 buffer with protease inhibitor cocktail, 10 micrograms of protein were separated by SDS-PAGE and transferred to PVDF membrane, blocked and blotted for two hours with PABP antibody in TBST, washed three times, secondary antibody for 1 hr (goat anti-mouse, Amersham, 1:10000). -
![Immunoprecipitation - Anti-PABP antibody [10E10] (ab6125)](https://www.abcam.cn/ps/products/6/ab6125/Images/ab6125-12038-anti-pabp-antibody-10e10-immunoprecipitation.jpg)
Immunoprecipitation - Anti-PABP antibody [10E10] (ab6125)PABP was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Mouse monoclonal to PABP (ab6125) 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, Hela whole cell extract 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 ab6125.
Secondary: Goat polyclonal to mouse IgG light chain specific (HRP) at 1/5000 dilution.
Band: 76kDa: PABP; 25kDa. -
![Flow Cytometry - Anti-PABP antibody [10E10] (ab6125)](https://www.abcam.cn/ps/products/6/ab6125/Images/ab6125-12036-anti-pabp-antibody-10e10-flow-cytometry.jpg)
Flow Cytometry - Anti-PABP antibody [10E10] (ab6125)Overlay histogram showing HeLa cells stained with ab6125 (red line). The cells were fixed with 100% methanol (5 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 (ab6125, 1µg/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 IgG2b [PLPV219] (ab91366, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in HeLa cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
文献 (29)
ab6125 被引用在 29 文献中.
- Yang X et al. Picornavirus 2A protease regulates stress granule formation to facilitate viral translation. PLoS Pathog 14:e1006901 (2018). PubMed: 29415027
- Haque N et al. ZFR coordinates crosstalk between RNA decay and transcription in innate immunity. Nat Commun 9:1145 (2018). PubMed: 29559679
- Xie X et al. Deubiquitylases USP5 and USP13 are recruited to and regulate heat-induced stress granules through their deubiquitylating activities. J Cell Sci 131:N/A (2018). PubMed: 29567855
- Booy EP et al. Comprehensive analysis of the BC200 ribonucleoprotein reveals a reciprocal regulatory function with CSDE1/UNR. Nucleic Acids Res 46:11575-11591 (2018). PubMed: 30247708
- Wakiyama M et al. MicroRNP-mediated translational activation of nonadenylated mRNAs in a mammalian cell-free system. Genes Cells 23:332-344 (2018). PubMed: 29626383
