重组Anti-SF3B1抗体[EPR11986] (ab172634)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR11986] to SF3B1
- Suitable for: Flow Cyt (Intra), IHC-P, WB, ICC/IF
- Reacts with: Mouse, Rat, Human
Related conjugates and formulations
概述
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产品名称
Anti-SF3B1抗体[EPR11986]
参阅全部 SF3B1 一抗 -
描述
兔单克隆抗体[EPR11986] to SF3B1 -
宿主
Rabbit -
经测试应用
适用于: Flow Cyt (Intra), IHC-P, WB, ICC/IFmore details
不适用于: IP -
种属反应性
与反应: Mouse, Rat, Human -
免疫原
Synthetic peptide within Human SF3B1 aa 1-100 (Cysteine residue). The exact sequence is proprietary.
Database link: O75533 -
阳性对照
- WB: HeLa, Jurkat, K562 and Ramos cell lysates. IHC-P: Human colon and glioma tissues. ICC/IF: HeLa cells. Flow Cyt (intra): HeLa cells.
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常规说明
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
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 long term. Avoid freeze / thaw cycle. -
存储溶液
pH: 7.20
Preservative: 0.01% Sodium azide
Constituents: 9% PBS, 40% Glycerol (glycerin, glycerine), 0.05% BSA, 50% Tissue culture supernatant -
Concentration information loading...
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纯度
Protein A purified -
克隆
单克隆 -
克隆编号
EPR11986 -
同种型
IgG -
研究领域
相关产品
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Alternative Versions
- HRP Anti-SF3B1 antibody [EPR11986] (ab202926)
- Anti-SF3B1 antibody [EPR11986] - BSA and Azide free (ab240170)
- Alexa Fluor® 488 Anti-SF3B1 antibody [EPR11986] (ab320190)
- Alexa Fluor® 647 Anti-SF3B1 antibody [EPR11986] (ab320191)
- Alexa Fluor® 555 Anti-SF3B1 antibody [EPR11986] (ab320192)
- Alexa Fluor® 594 Anti-SF3B1 antibody [EPR11986] (ab320193)
- PE Anti-SF3B1 antibody [EPR11986] (ab320194)
- APC Anti-SF3B1 antibody [EPR11986] (ab320195)
- Alexa Fluor® 750 Anti-SF3B1 antibody [EPR11986] (ab321172)
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Compatible Secondaries
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Isotype control
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Positive Controls
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab172634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 (Intra) |
1/2000.
|
|
IHC-P |
1/100 - 1/250. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
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|
WB |
1/1000 - 1/10000. Predicted molecular weight: 146 kDa.
|
|
ICC/IF |
1/200 - 1/500.
|
说明 |
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Flow Cyt (Intra)
1/2000. |
IHC-P
1/100 - 1/250. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
WB
1/1000 - 1/10000. Predicted molecular weight: 146 kDa. |
ICC/IF
1/200 - 1/500. |
靶标
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相关性
SF3B1 is subunit 1 of the splicing factor 3b protein complex. Splicing factor 3b, together with splicing factor 3a and a 12S RNA unit, forms the U2 small nuclear ribonucleoproteins complex (U2 snRNP). The splicing factor 3b/3a complex binds pre-mRNA upstream of the intron's branch site in a sequence independent manner and may anchor the U2 snRNP to the pre-mRNA. Splicing factor 3b is also a component of the minor U12-type spliceosome. The carboxy-terminal two-thirds of subunit 1 have 22 non-identical, tandem HEAT repeats that form rod-like, helical structures. -
细胞定位
Nucleus speckle. Note=During mitosis, transiently dispersed from the nuclear speckles to the cytoplasm. -
数据库链接
- Entrez Gene: 23451 Human
- Entrez Gene: 81898 Mouse
- Entrez Gene: 84486 Rat
- Omim: 605590 Human
- SwissProt: O75533 Human
- SwissProt: Q99NB9 Mouse
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别名
- Hsh 155 antibody
- MDS antibody
- Pre mRNA processing 10 antibody
see all
图片
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All lanes : Anti-SF3B1 antibody [EPR11986] (ab172634) at 1/1000 dilution
Lane 1 : RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) whole cell lysate
Lane 2 : PC-12 (rat adrenal gland pheochromocytoma cell) whole cell lysate
Lane 3 : NIH/3T3 (mouse embryonic fibroblast) whole cell lysate
Lane 4 : C6 (rat glial tumor glial cell) whole cell lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 146 kDa
Observed band size: 146 kDaBlocking/Diluting buffer and concentration: 5% NFDM/TBST
Exposure time:
Lane 1-3: 3.25 seconds
Lane 4: 15 seconds -
Immunocytochemistry/ Immunofluorescence analysis of NIH/3T3 (mouse embryonic fibroblast) labeling SF3B1 with ab172634 at 1/200 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Cells were fixed with 4% Paraformaldehyde and permeabilised with 0.1% TritonX-100. Nuclear counterstain was DAPI. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) at 1/200 was used as counterstain antibody.
Confocal image showing nuclear staining in NIH/3T3 cell line.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). -
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SF3B1 antibody [EPR11986] (ab172634)
Immunohistochemical analysis of Formalin-fixed, paraffin-embedded Human colon tissue labeling SF3B1 with ab172634 at 1/100 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
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Intracellular Flow Cytometry analysis of HeLa (human cervix adenocarcinoma) cells labeling SF3B1 (red) with ab172634 at a 1/2000 dilution. Cells were fixed with 4% paraformaldehyde and permeabilized with 90% methanol. A goat anti-rabbit IgG (Alexa Fluor® 488) (ab150077) was used as the secondary antibody at a 1/2000 dilution. Black - Rabbit monoclonal IgG (ab172730). Blue (unlabeled control) - Cells without incubation with the primary and secondary antibodies.
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Immunocytochemistry/ Immunofluorescence analysis of HeLa (human cervical adenocarcinoma epithelial cell) labeling SF3B1 with ab172634 at 1/200 dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 dilution. Cells were fixed with 4% Paraformaldehyde and permeabilised with 0.1% TritonX-100. Nuclear counterstain was DAPI. ab195889 Anti-alpha Tubulin mouse monoclonal antibody - Microtubule Marker (Alexa Fluor® 594) at 1/200 was used as counterstain antibody.
Confocal image showing nuclear staining in Hela cell line.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8). -
All lanes : Anti-SF3B1 antibody [EPR11986] (ab172634) at 1/1000 dilution
Lane 1 : HeLa (human cervical adenocarcinoma epithelial cell) nuclear fraction
Lane 2 : HeLa (human cervical adenocarcinoma epithelial cell) cytoplasmic fraction
Lane 3 : PC-12 (rat adrenal gland pheochromocytoma cell) nuclear fraction
Lane 4 : PC-12 (rat adrenal gland pheochromocytoma cell) cytoplasmic fraction
Lane 5 : RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) nuclear fraction
Lane 6 : RAW 264.7 (mouse Abelson murine leukemia virus-induced tumor macrophage) cytoplasmic fraction
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/20000 dilution
Predicted band size: 146 kDa
Observed band size: 145 kDa why is the actual band size different from the predicted?Blocking/Diluting buffer and concentration: 5% NFDM/TBST
Exposure time:
Lane 1-4: 1 second
Lane 5-6: 10 secondsIn Western blot, anti- H3 antibody (ab176842) loading control staining at 1/100000 dilution and anti-GAPDH antibody (ab181602) loading control staining at 1/200000 dilution.
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All lanes : Anti-SF3B1 antibody [EPR11986] (ab172634) at 1/1000 dilution
Lane 1 : HeLa lysate
Lane 2 : Jurkat lysate
Lane 3 : K562 lysate
Lane 4 : Ramos lysate
Lysates/proteins at 10 µg per lane.
Predicted band size: 146 kDa -
Immunofluorescence analysis of HeLa cells labeling SF3B1 with ab172634 at 1/250 dilution.
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SF3B1 antibody [EPR11986] (ab172634)
Immunohistochemical analysis of Formalin-fixed, paraffin-embedded Human glioma tissue labeling SF3B1 with ab172634 at 1/100 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
实验方案
数据表及文件
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SDS download
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Datasheet download
文献 (14)
ab172634 被引用在 14 文献中.
- Fuentes-Fayos AC et al. SF3B1 inhibition disrupts malignancy and prolongs survival in glioblastoma patients through BCL2L1 splicing and mTOR/ß-catenin pathways imbalances. J Exp Clin Cancer Res 41:39 (2022). PubMed: 35086552
- Simmler P et al. SF3B1 facilitates HIF1-signaling and promotes malignancy in pancreatic cancer. Cell Rep 40:111266 (2022). PubMed: 36001976
- Zhang M et al. Neural stemness unifies cell tumorigenicity and pluripotent differentiation potential. J Biol Chem 298:102106 (2022). PubMed: 35671824
- Rouf Banday A et al. Targeting natural splicing plasticity of APOBEC3B restricts its expression and mutagenic activity. Commun Biol 4:386 (2021). PubMed: 33753867
- Yang JY et al. SF3B1 mutation in pancreatic cancer contributes to aerobic glycolysis and tumor growth through a PP2A-c-Myc axis. Mol Oncol 15:3076-3090 (2021). PubMed: 33932092