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当前位置: 首页 > 产品中心 > Functional_antibody > Cusabio/His-Tag Monoclonal Antibody/100μg/CSB-MA000159
商品详细Cusabio/His-Tag Monoclonal Antibody/100μg/CSB-MA000159
Cusabio/His-Tag Monoclonal Antibody/100μg/CSB-MA000159
Cusabio/His-Tag Monoclonal Antibody/100μg/CSB-MA000159
商品编号: CSB-MA000159
品牌: Cusabio
市场价: ¥3340.00
美元价: 1670.00
产地: 美国(厂家直采)
公司:
产品分类: 功能性抗体
公司分类: Functional_antibody
联系Q Q: 3392242852
电话号码: 4000-520-616
电子邮箱: info@ebiomall.com
商品介绍

His-Tag Monoclonal Antibody

Datasheet
CodeCSB-MA000159
SizeUS$167
Image
  • IP antibody use: 5µg His Mouse IgG1 per ml Lysate, WB 1:3000Lane 1: untransfected 293 cell lysateLane 2: transfected 293 cell lysate with His-tag fusion proteinLane 3: IP (untransfected 293 + anti-His mAb + Protein G agarose)Lane 4: IP (transfected 293 + normal Mouse IgG + Protein G agarose)Lane 5: IP (transfected 293 + anti-His mAb + Protein G agarose)Lane 6: Recombinant protein (E.coli)

  • IF analysis of 293 cells transfected with a His-tag protein,1:1000 dilution (blue DAPI, red anti-His)

  • 2µgHis fusion protein + Primary antibody dilution at1) 1:5000 2) 1:10000

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Product Details

Description
His-Tag monoclonal antibody CSB-MA000159 was produced in mouse immunized by using Synthetic Peptide as the immunogen. The immunogen is a short peptide. It is specifically designed for the adsorptive purification of recombinant proteins. The relatively small size of His tags makes its integration into expression vectors extremely easy.This His-Tag Monoclonal Antibody was tested in the WB, IF, IP and ELISA applications. An efficient detection and purification system based on fusion proteins can be established using the His tag. It can be used for detection and expression of His-tag fusion expression proteins, intracellular localization, and purification, qualitative or quantitative detection of His fusion-expressed proteins and the like. It doesn’t have species restricted.
Target NamesHis-Tag
Raised inMouse
Species ReactivityN/A
ImmunogenSynthetic Peptide
ConjugateNon-conjugated
IsotypeIgG
ConcentrationIt differs from different batches. Please contact us to confirm it.
BufferPBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.
FormLiquid
Tested ApplicationsELISA, WB, IF, IP
Recommended Dilution
ApplicationRecommended Dilution
WB1:500-1:5000
IF1:50-1:200
IP1:200-1:2000
ProtocolsELISA ProtocolWestern Blotting(WB) ProtocolImmunofluorescence (IF) ProtocolImmunoprecipitation (IP) Protocol
Troubleshooting and FAQsAntibody FAQs
StorageUpon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead TimeBasically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.

Citations

Somatic SF3B1 hotspot mutation in prolactinomas. C Li,Nature Communications,2020

Applications: GST pull-downAntibody dilution factor: 1:200Review: We examined Pit-1 protein binding in relation to ESRRG alternative splicing status. Pit-1 protein fused to glutathione S-transferase (GST) pull-down HIS-tagged cryptic ESRRG, whereas it bound weakly to canonical ESRRG PMID: 32427851

When spider and snake get along: Fusion of a snake disintegrin with a spider phospholipase D to explore their synergistic effects on a tumor cell. Siqueira RAGB, et al,Toxicon,2019

Applications: ELISAAntibody dilution factor: 1: 4000Review: Murine B16F10 and L929 cell lines (2× 10 5 ) were fixed on plates and then blocked with 2% BSA solution. After that, Rechistatin, Echistatin, LgRec1 or EGFP (1; 3; 6 and 9μM) were added to the plates followed by incubation for 2 h at 37°C. The binding of the recombinant proteins to the cells was assessed using anti-His (Cusabio®) mAb followed by anti-mouse IgG-peroxidase conjugate (Sigma® ). The reaction was measured by spectrophotometer at 492 nm, the higher the absorbance the grater the binding of the toxins to the cells. A) Binding of recombinant toxins on murine B16F10 melanoma cells; B) Binding of recombinant toxins on murine L929 cells. The results were expressed as mean ± SD (n = 3), ***p < 0.001;="">**p < 0.01="" and="">*p < 0.05="" comparing="" rechistatin,="" echistatin,="" lgrec1="" and="" egfp="" groups="" com-="" pared="" with="">PMID: 31251993

Subfunctionalization of the Ruby2-Ruby1 gene cluster during the domestication of citrus. Huang D, et al,Nature Plants,2018

Application: Pull-down assayReview: Competitive binding assays of CgRuby1 and CgRuby2Short binding to CgbHLH1. The mixture of HIS-CgRuby1 and FLAG CgRuby2Short was added to immobilized GSTCgbHLH1. The precipitates were detected using western blot analysis with anti-HIS, anti-FLAG or anti-GST antibodies. The gradient indicates the increasing amount of FLAG-CgRuby2Short. These experiments were repeated independently twice with similar results.PMID: 30374094

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品牌介绍
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