Anti-Myc tag抗体(ab9106)
Key features and details
- Rabbit polyclonal to Myc tag
- Suitable for: IHC-Fr, IP, WB, IHC-P, ICC/IF, Electron Microscopy
- Reacts with: Species independent
- Isotype: IgG
选择批间可重复性更高的重组抗体
- 研究可靠 —— 各批次间结果一致且可重复
- 长期批量供应 —— 采用重组技术,可实现快速生产
- 首次实验即可成功 —— 经过大量验证确认了特异性
- 符合伦理标准 —— 产品不含动物成分
概述
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产品名称
Anti-Myc tag抗体
参阅全部 Myc tag 一抗 -
描述
兔多克隆抗体to Myc tag -
宿主
Rabbit -
特异性
ELISA: Antibody specificity was verified by ELISA against the peptide (EQKLISEEDL). A 1:60,000 dilution of the antibody gave an O.D.=1.0 in a 15 minute reaction using HRP-conjugated Goat Anti Rabbit IgG at 1:20,000 and TMB as the substrate. Appropriate specificity controls were run. -
经测试应用
适用于: IHC-Fr, IP, WB, IHC-P, ICC/IF, Electron Microscopymore details -
种属反应性
与反应: Species independent -
免疫原
Synthetic peptide corresponding to Myc tag conjugated to keyhole limpet haemocyanin.
(Peptide available asab13837) -
阳性对照
- ICC/IF: CHO cells transfected with 12-tags constructs. IHC-P: Mouse brain tissue stained for Myc tag. EM: Mouse embryonic fibroblasts expressing myc-tagged protein. IP: Huh7 expressing myc-tagged CDC42 protein and transfected 293FT cells. WB: Y. enterocolitica ?HOPEMT carrying plasmids encoding Myc-tagged CT082 or CT695, and HA-tagged Slc1.
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常规说明
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
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 -
Concentration information loading...
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纯度
Affinity purified -
纯化说明
Antibodies were immunoaffinity purified using the peptide immobilized on a solid phase. Antibody concentration was determined by extinction coefficient : O.D. 1.4 at 280nM equals 1.0 mg of IgG. -
克隆
多克隆 -
同种型
IgG -
研究领域
相关产品
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Assay kits
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Compatible Secondaries
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Conjugation kits
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Isotype control
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Related Products
应用
应用 | Ab评论 | 说明 |
---|---|---|
IHC-Fr | (1) |
1/500.
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IP | (9) |
Use at an assay dependent concentration.
|
WB | (14) |
Use at an assay dependent concentration.
|
IHC-P | (3) |
Use at an assay dependent concentration.
|
ICC/IF | (10) |
1/1000.
|
Electron Microscopy |
Use at an assay dependent concentration. See Abreview for further details (submitted by Eeva-Liisa Eskelinen).
|
说明 |
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IHC-Fr
1/500. |
IP
Use at an assay dependent concentration. |
WB
Use at an assay dependent concentration. |
IHC-P
Use at an assay dependent concentration. |
ICC/IF
1/1000. |
Electron Microscopy
Use at an assay dependent concentration. See Abreview for further details (submitted by Eeva-Liisa Eskelinen). |
靶标
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相关性
Epitope tags are short peptide sequences that are easily recognized by tag-specific antibodies. Due to their small size, epitope tags do not affect the tagged protein’s biochemical properties. Most often sequences encoding the epitope tag are included with target DNA at the time of cloning to produce fusion proteins containing the epitope tag sequence. This allows anti-epitope tag antibodies to serve as universal detection reagents for any tag containing protein produced by recombinant means. This means that anti-epitope tag antibodies are a useful alternative to generating specific antibodies to identify, immunoprecipitate or immunoaffinity purify a recombinant protein. The anti-epitope tag antibody is usually functional in a variety of antibody-dependent experimental procedures. Expression vectors producing epitope tag fusion proteins are available for a variety of host expression systems including bacteria, yeast, insect and mammalian cells. -
细胞定位
Nuclear -
别名
- c-myc tag antibody
- Myc Epitope Tag antibody
图片
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Immunofluorescent analysis of 4% paraformaldehyde (PFA)-fixed, permeabilized with 0.1% Triton X-100 in CHO cells transfected with 12-tags constructs (named as CHO-12 tags, Top) and parental CHO cells (Bottom) labelling MYC with ab9106 at 1/1000 dilution (1 μg/mL), followed by Donkey Anti-rabbit IgG (H&L), FITC conjugated antibody at 1/1000 dilution (1 μg/mL) (Green). Nucleus was counterstained with DAPI (Blue).
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Y. enterocolitica ΔHOPEMT carrying plasmids encoding Myc-tagged CT082 or CT695, and HA-tagged Slc1 (as indicated) were grown in non-secreting conditions. Chloramphenicol was added (time?=?0 min) to stop bacterial protein synthesis and samples were taken at the indicated time points. Samples were analyzed by immunoblotting using ab9106, anti-HA, and anti-TEM antibodies.
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ab9106 at 4 µg/mg lysate used in Huh7 (Human cell line) whole cell lysate (1x106 cells).
Cells expressed myc-tagged CDC42 protein. Immunoprecipitation step performed using Protein A matrix. Incubation time 4 hours at 4°C. Western Blot antibody used at 1/300 dilution.
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ab9106 used at 1/250 in the immunoprecipitation of transfected human 293FT cells (whole cell lysate).
In this experiment cells were co-transfected with myc tagged cdc25 along with an HA tagged viral protein which binds to cdc25. The cell lysate was immunoprecipitated using ab9106, run on a 10% gel. The blot was probed for HA and HA tagged protein (which co-IPed with Myc tagged protein) and this is seen at ~15KDa.
Lane 1: Input non-transfected cells
Lane 2: Immunoprecipitated non-transfected cells
Lane 3: Input co-transfected cells
Lane 4: Immunoprecipitated co-transfected cells
This image is courtesy of an Abreview submitted on 23 March 2006.
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Paraformaldehyde-fixed frozen mouse brain tissue stained for Myc tag using ab9106 at a 1/500 dilution (2hrs at 25°C), followed by a goat anti-rabbit Alexa-Fluor® 568 secondary used at a 1/500 dilution.
For further details please see abreview.
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Paraformaldehyde-fixed, 0.3% Triton X-100 permeabilized mouse brain tissue stained for Myc tag using ab9106 at a 1/500 dilution (15 hrs, 4°C) followed by and Alexa-Fluor® 555 donkey anti-rabbit secondary used at a 1/500 dilution.
For further details please see abreview.
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ab9106 at 1/2000 staining mouse embryonic fibroblasts expressing myc-tagged protein by ICC.
The cells were paraformaldehyde fixed and blocked with 3% BSA prior to incubation with the antibody for 1 hour. A goat anti-rabbit IgG antibody (10 nm gold conjugated) was used as the secondary.
The image shown is immuno electron microscopical staining with thawed cryosections.
实验方案
数据表及文件
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SDS download
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Datasheet download
文献 (472)
ab9106 被引用在 472 文献中.
- Yuan L et al. The ubiquitin ligase RNF2 stabilizes ERα and modulates breast cancer progression. Hum Cell 36:353-365 (2023). PubMed: 36271315
- Binda O et al. SMA-linked SMN mutants prevent phase separation properties and SMN interactions with FMRP family members. Life Sci Alliance 6:N/A (2023). PubMed: 36375840
- Liu F et al. circRNF10 Regulates Tumorigenic Properties and Natural Killer Cell-Mediated Cytotoxicity against Breast Cancer through the miR-934/PTEN/PI3k-Akt Axis. Cancers (Basel) 14:N/A (2022). PubMed: 36497344
- Yang H et al. RNF31 represses cell progression and immune evasion via YAP/PD-L1 suppression in triple negative breast Cancer. J Exp Clin Cancer Res 41:364 (2022). PubMed: 36581998
- Barber KW et al. CasPlay provides a gRNA-barcoded CRISPR-based display platform for antibody repertoire profiling. Cell Rep Methods 2:100318 (2022). PubMed: 36313802