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Cell Biology Proteolysis / Ubiquitin Proteasome / Ubiquitin Sumo

Anti-Sumo 1抗体(ab5316)

  • Datasheet
Reviews (1)Q&A (3)References (29)

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Key features and details

  • Rabbit polyclonal to Sumo 1
  • Suitable for: WB
  • Reacts with: Arabidopsis thaliana
  • Isotype: IgG

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Recombinant human Sumo 1 protein (ab3801)

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概述

  • 产品名称

    Anti-Sumo 1抗体
    参阅全部 Sumo 1 一抗
  • 描述

    兔多克隆抗体to Sumo 1
  • 宿主

    Rabbit
  • 经测试应用

    适用于: WBmore details
  • 种属反应性

    与反应: Arabidopsis thaliana
  • 免疫原

    Recombinant full length protein (Arabidopsis thaliana).

  • 阳性对照

    • Arabidopsis extracts that have been heat treated for for 30-120 mins by moving them from 24 to 37 degrees C. Recombinant SUMO1 is detectable at concentrations as low as 5ng/ml.
  • 常规说明

    Reproducibility is key to advancing scientific discovery and accelerating scientists’ next breakthrough.

    Abcam is leading the way with our range of recombinant antibodies, knockout-validated antibodies and knockout cell lines, all of which support improved reproducibility.

    We are also planning to innovate the way in which we present recommended applications and species on our product datasheets, so that only applications & species that have been tested in our own labs, our suppliers or by selected trusted collaborators are covered by our Abpromise™ guarantee.

    In preparation for this, we have started to update the applications & species that this product is Abpromise guaranteed for.

    We are also updating the applications & species that this product has been “predicted to work with,” however this information is not covered by our Abpromise guarantee.

    Applications & species from publications and Abreviews that have not been tested in our own labs or in those of our suppliers are not covered by the Abpromise guarantee.

    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, as well as customer reviews and Q&As.

性能

  • 形式

    Liquid
  • 存放说明

    Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
  • Concentration information loading...
  • 纯度

    Whole antiserum
  • 克隆

    多克隆
  • 同种型

    IgG
  • 研究领域

    • Cell Biology
    • Proteolysis / Ubiquitin
    • Proteasome / Ubiquitin
    • Sumo
    • Cardiovascular
    • Heart
    • Autophagy
    • APG gene products
    • Metabolism
    • Pathways and Processes
    • Metabolism processes
    • Autophagy and mitophagy
    • APG gene products
    • Cancer
    • Cell Death
    • Autophagy
    • APG gene products

相关产品

  • Compatible Secondaries

    • Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) (ab150077)
    • Goat Anti-Rabbit IgG H&L (HRP) (ab205718)
  • Isotype control

    • Rabbit IgG, polyclonal - Isotype Control (ChIP Grade) (ab171870)
  • Recombinant Protein

    • Recombinant human Sumo 1 protein (ab3801)

应用

Our Abpromise guarantee covers the use of ab5316 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 1/1000. Predicted molecular weight: 12 kDa.

靶标

  • 功能

    Ubiquitin-like protein that can be covalently attached to proteins as a monomer or a lysine-linked polymer. Covalent attachment via an isopeptide bond to its substrates requires prior activation by the E1 complex SAE1-SAE2 and linkage to the E2 enzyme UBE2I, and can be promoted by E3 ligases such as PIAS1-4, RANBP2 or CBX4. This post-translational modification on lysine residues of proteins plays a crucial role in a number of cellular processes such as nuclear transport, DNA replication and repair, mitosis and signal transduction. Involved for instance in targeting RANGAP1 to the nuclear pore complex protein RANBP2. Polymeric SUMO1 chains are also susceptible to polyubiquitination which functions as a signal for proteasomal degradation of modified proteins. May also regulate a network of genes involved in palate development.
  • 疾病相关

    Defects in SUMO1 are the cause of non-syndromic orofacial cleft type 10 (OFC10) [MIM:613705]; also called non-syndromic cleft lip with or without cleft palate 10. OFC10 is a birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. Note=A chromosomal aberation involving SUMO1 is the cause of OFC10. Translocation t(2;8)(q33.1;q24.3). The breakpoint occurred in the SUMO1 gene and resulted in haploinsufficiency confirmed by protein assays.
  • 序列相似性

    Belongs to the ubiquitin family. SUMO subfamily.
    Contains 1 ubiquitin-like domain.
  • 翻译后修饰

    Cleavage of precursor form by SENP1 or SENP2 is necessary for function.
    Polymeric SUMO1 chains undergo polyubiquitination by RNF4.
  • 细胞定位

    Nucleus membrane. Nucleus speckle. Cytoplasm. Recruited by BCL11A into the nuclear body.
  • Target information above from: UniProt accession P63165 The UniProt Consortium
    The Universal Protein Resource (UniProt) in 2010
    Nucleic Acids Res. 38:D142-D148 (2010) .

    Information by UniProt
  • 别名

    • DAP1 antibody
    • GAP modifying protein 1 antibody
    • GAP-modifying protein 1 antibody
    • GMP 1 antibody
    • GMP1 antibody
    • OFC10 antibody
    • PIC 1 antibody
    • PIC1 antibody
    • SENP2 antibody
    • Sentrin 1 antibody
    • Sentrin antibody
    • Small ubiquitin related modifier 1 antibody
    • Small ubiquitin-like modifier 1 antibody
    • Small ubiquitin-related modifier 1 antibody
    • SMT3 antibody
    • SMT3 homolog 3 antibody
    • SMT3 suppressor of mif two 3 homolog 1 antibody
    • SMT3, yeast, homolog 3 antibody
    • Smt3C antibody
    • SMT3H3 antibody
    • SUMO-1 antibody
    • SUMO1 antibody
    • SUMO1_HUMAN antibody
    • Ubiquitin homology domain protein PIC1 antibody
    • Ubiquitin Like 1 antibody
    • Ubiquitin like protein SMT3C antibody
    • Ubiquitin like protein UBL1 antibody
    • Ubiquitin-homology domain protein PIC1 antibody
    • Ubiquitin-like protein SMT3C antibody
    • Ubiquitin-like protein UBL1 antibody
    • UBL 1 antibody
    • UBL1 antibody
    see all

实验方案

  • Western blot protocols

Click here to view the general protocols

数据表及文件

    • Datasheet
  • 文献 (29)

    发表研究结果有使用 ab5316?请让我们知道,以便我们可以引用本数据表中的参考文章。

    ab5316 被引用在 29 文献中.

    • Lin J  et al. UL36 Encoded by Marek's Disease Virus Exhibits Linkage-Specific Deubiquitinase Activity. Int J Mol Sci 21:N/A (2020). PubMed: 32150874
    • Liu Y  et al. Defining the function of SUMO system in pod development and abiotic stresses in Peanut. BMC Plant Biol 19:593 (2019). PubMed: 31884953
    • Wang H  et al. Overexpression of a maize SUMO conjugating enzyme gene (ZmSCE1e) increases Sumoylation levels and enhances salt and drought tolerance in transgenic tobacco. Plant Sci 281:113-121 (2019). PubMed: 30824044
    • Niu  et al. SIZ1-Mediated SUMOylation of TPR1 Suppresses Plant Immunity in Arabidopsis. Mol Plant 12:215-228 (2019). PubMed: 30543996
    • Wang H  et al. The Maize Class-I SUMO Conjugating Enzyme ZmSCE1d Is Involved in Drought Stress Response. Int J Mol Sci 21:N/A (2019). PubMed: 31861556
    View all Publications for this product

    客户评价及客户问答

    Show All 评价 Q&A
    提交评价 提交问题

    1-4 of 4 Abreviews or Q&A

    Western blot abreview for Anti-Sumo 1 antibody

    Good
    Abreviews
    Abreviews
    abreview image
    Application
    Western blot
    Sample
    Plants Tissue lysate - whole (anther)
    Loading amount
    30 µg
    Specification
    anther
    Gel Running Conditions
    Non-reduced Denaturing
    Blocking step
    Milk as blocking agent for 12 hour(s) and 0 minute(s) · Concentration: 5% · Temperature: 4°C
    Read More

    Abcam user community

    Verified customer

    提交于 Dec 05 2012

    Question

    Customer is not seeing a signal in WB with her most recent order for ab5316. The previous vial that she used worked very well and she did a side by side comparison. Order# 101464. Previous order 90661.

    Read More

    Abcam community

    Verified customer

    Asked on Oct 28 2005

    Answer

    Thank you for your phone call and I'm sorry to hear that you are experiencing difficulty with ab5316. The replacement vials are being sent to your attention free of charge on order reference # 109485. The item is currently out of stock and so you should receive it early next week. You will receive emails regarding shipping to keep you updated. Please let me know how the replacement works out for you and if you have any additional questions.

    Read More

    Abcam Scientific Support

    回复于 Oct 31 2005

    Question

    I tested the antibody first with my protein extract on SDS-PAGE. I found a very high non-specific background to the membrane. Subsequently, i did not apply any protein sample to my test membrane for troubleshooting. Therefore, i don't think it would be protein degradation or amount of protein or % of gel that caused the background problem since i have not used any of these in my testing. The image that i sent you was just empty clean membranes with no protein on it and as you can see, the antibody bound extremely well onto the membrane even i have use either 10% milk or 5% BSA to block it overnight before applying the antibody. Look forward to your suggestions Thanks

    Read More

    Abcam community

    Verified customer

    Asked on May 20 2005

    Answer

    Thank you for getting back to me and for providing further information about your experiments. As we understand from your recent e-mail, after blocking the membrane (without running the samples) the primary antibody provided a very high background signal. Have you tested the secondary antibody alone (run a secondary control only) to see if this problem really comes from the primary or the secondary antibody? I have checked your order record and the delivery details in our system. Looking at FedEx website I can see that the package was held up at the customs for several days. It may well be that the antibody has just gone off during long delivery. We have the same batch in stock at the moment but I can send you a new vial from the same Lot (free of charge) if you wish to test it. Please get back to me and do let me know how to process. I am looking forward to hearing from you soon.

    Read More

    Abcam Scientific Support

    回复于 May 24 2005

    Question

    1. Order details: •Batch number:lot 25213 •Abcam order or Purchase order number: order ref no. 81493 •Antibody storage conditions (temperature/reconstitution etc): 2. Please describe the problem (high background, wrong band size, more bands, no band etc). very high background. I have troubleshoot by using empty membranes (PVDF and nitrocelullose) without any protein samples, the signal is so high that the membrane glow in the dark. 3. On what material are you testing the antibody in WB? •Species: Aspergillus nidulans •Cell extract or Nuclear extract: Crude extract •Purified protein or Recombinant protein: 3. The lysate •How much protein was loaded: 50ug •What lysis buffer was used: Tris, SDS •What protease inhibitors were used: none •What loading buffer was used: Lammeli •Did you heat the samples: temperature and time: yes, boil for 3mins 4. Electrophoresis/Gel conditions/ Transfer conditions •Reducing or non reducing gel: reducing •Gel percentage : 8% •Transfer conditions: semi-dry 5. Blocking conditions •Buffer:TBS-T •Blocking agent: milk, BSA, serum, what percentage: Tried 5%, 10% milk, 5% BSA •Incubation time:for a few hours to overnight •Incubation temperature:25oC 6. Primary Antibody •Specification (in which species was it raised against): Rabbit •At what dilution(s) have you tested this antibody: 1:1000 as recommended •What dilution buffer was used:5%milk in TBS-T •Incubation time:1hr at 25oC or O/N at 4oC •Incubation temperature:4 and 25 oC tested •What washing steps were done:3x 10 mins with TBS-T 7. Secondary Antibody •Specification (in which species was it raised against)? Goat •At what dilution(s) have you tested this antibody:1/5000 •Incubation time 1hr at 4oC •Wash steps:3x10mins with TBS-T •Do you know whether the problems you are experiencing come from the secondary? It is working fine with my other westerns 8. Detection method ECl, ECl+, other detection method: ECL+ 9. Background bands •Have you eliminated the possibility that any background bands could be due to the secondary antibody? (Run a “No primary” control): other westerns work fine •Is the blocking step sufficient? yes (10% milk overnight) •Are your washing steps sufficiently stringent? (Multiple short washes are more effective than fewer longer wash steps) I have tried that too... •At what size are the bands migrating? Could they be degradation products of your target? empty membrane has high background too •Please provide an image of your blot (as an e-mail attachment, a faxed image is not sufficient) 10. Did you apply positive and negative controls along with the samples? Please specify. 11. Optimization attempts •How many times have you tried the Western? at least 5 times •Do you obtain the same results every time e.g. are background bands always in the same place? background everywhere even with empty membrane •What steps have you altered? empty (no protein) nitrocelluse and PVDF, respectively

    Read More

    Abcam community

    Verified customer

    Asked on May 17 2005

    Answer

    Thank you for contacting us and for taking your time to fill in the Questionnaire and for providing more information about your Western blot assay. This antibody was raised against a recombinant full length protein from Arabidopsis thaliana and it has been characterized using samples from this species. Unfortunately, other species have not been tested yet and we do not know if ab5316 recognizes Sumo 1 in Aspergillus nidulans or not. Here we would like to make some suggestions which could improve the detection: As we understand from your e-mail, you do not use any proteinase inhibitors in the lysis buffer when preparing the samples. It is very important to apply a cocktail of different proteinases in order to prevent the degradation of the target. It is difficult to tell what may have happened in your samples without seeing the Wb image but it may well be that the high background due to protein degradation. You loaded 50 ug of protein onto the gel which is a bit too much. We usually advise 20-30 ug per lane, otherwise the gel is simply overloaded. The excepted band size is 12 kDa. In order to be able to detect a band at such a low MW level, you need to apply high percentage of gel i.e. 15%. If you use 8%, there is a very high chance that the separated target protein has run out of the gel. We hope that this information will be useful for you.

    Read More

    Abcam Scientific Support

    回复于 May 19 2005

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