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BSG/AlbuVoid™ PLUS - Albumin and IgG Depletion From Serum/Plasma for Proteomics/NP-AVK-05
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产品说明
Albumin and IgG Depletion From Serum/Plasma for ProteomicsIgG removal >90% (70-80% of total Immunoglobulins removed)Albumin removal >95%Seamless and simple < 1 hour protocolLow abundance enrichment equivalent to immuno-affinityDisposable, cost-effective, no column regeneration or cross-contaminationWorks for most species tested including human, sheep, rat, mouse, bovineOn-bead protocols improve workflow and efficiency, especially suited to targeted proteomicsSuitable for LC-MS, 1 and 2D Gels, ELISAs, Enzyme and other Functional Assays.The classical plasma proteins generally fall into functional categories, forming the vast majority of the mid-to-high abundance proteome. In serum, these sub-proteomes by mass content are: Albumin 50-60%; Immunoglobulins 10-20%; Transport Proteins (Transferrin, Apo) 5-10%; Complement related Proteins 3-5%; Protease Inhibitors 2-5%; and all others 2-5%. While these sub-proteomes are required for normal body homeostasis, they nevertheless can become dysfunctional during acute-phase and chronic stimuli.So, depending on the needs of the investigation, it can be valuable to consider that one or more of these categorical sub-proteomes is simply background noise whereby depletion is beneficial. While in other cases, these same categorical sub-proteomes might provide new data and information and consequently, should not be depleted. Different AlbuVoid™, AlbuVoid™ PLUS and AlbuSorb™ PLUS workflows support different proteomic biases as outlined in the following Table.Products and digest conditions produce different sub-proteome windows of observation. So, depending on the needs of the investigation, it can be valuable to consider that one or more of these categorical sub-proteomes is simply background noise whereby depletion is beneficial. While in other cases, these same categorical sub-proteomes might provide new data and information and consequently, should not be depleted. Categorically the acute-phase sub-proteomes differentiated in disease may vary greatly from those associated with chronic sub-proteomes. So there is great benefit in having options to enrich or deplete one or more of these sub-proteomes.BSG"s Albumin and IgG Removal Kits offer many such options:The "PLUS" products substantially deplete Immunoglobulins through separations at the protein level.The variable regions of Immunoglobulins are extremely heterogeneous, generating a background noise across the full LC gradient. On-bead digestion (BASP™) with AlbuVoid™ substantially reduces the influence of such Ig peptide features. So in addition to workflow simplicity, BASP™ can be advantageous utilized in targeted proteomic workflows whenever the target proteins do not require strong denaturing conditions.With the exception of Immunoglobulins whereby FASP generates many more spectral features, both strong denaturing conditions (FASP) and on-bead digest (BASP™) conditions produce similar protein profiles.Both Apolipoproteins and heavily glycosylated proteins (i.e., α1-Acid Glycoprotein) bind poorly to AlbuVoid™. For quantitative studies within these classes of proteins, AlbuSorb™ PLUS is recommended.The Complement sub-proteome is especially enriched by AlbuVoid™ PLUS. The digest conditions may bias towards one or more functional sub-populations, likely due to conformational transitions and protein-protein interactions (i.e., Factor Bb, Properdin) that occur upon activation. This needs further investigation.The low abundance sub-proteome is enriched 5+ fold with AlbuVoid™ and 4+ fold with AlbuSorb™ PLUS.ProductSize# Serum PrepsItem No.AlbuVoid™ PLUS Kit5 preps5,25µl Serum samplesNP-AVK-05AlbuVoid™ PLUS Kit10 preps10,25µl Serum samplesNP-AVK-10Click Here For The AlbuVoid™ Plus Product Sheet.

    美国BSG(Biotech Support Group''LLC)公司是一家公司是一家全球知名的蛋白质组和基因组样本预处理的公司,是这个领域公认的领导者,该公司将其发明的专利表面化学技术应用生物学领域,比其他方法如亲合技术,苯酚法有绝对的优势。由于技术上的领先,使得BSG公司的产品广泛被美国国家基因组研究所,斯坦福大学等重要机构使用。(http://www.biotechsupportgroup.com/)

    Nature Article Cites HemogloBind™ and NRicher™ for Macromolecular Complex Annotation

    MONMOUTH JUNCTION, NJ, February 9, 2016 -- Biotech Support Group reports on a recent research article published in Nature, describing the simplicity and efficiency of their proteomic enrichment technology to observe and annotate soluble multiprotein complexes common to metazoa.


    The citation is:

    C Wan, B BorgesonS Phanse, F Tu, K DrewG Clark, et al. Panorama of ancient metazoan macromolecular complexesNature 525339–344 (17 September 2015).

    doi:10.1038/nature14877


    In brief, the article’s authors aimed at 
    elucidating the components of multiprotein complexes on a proteome-wide scale. The authors identify protein complexes from nine species in parallel, based on biochemical fractionation of native soluble macromolecular complexes followed by tandem mass spectrometry to identify components. The article states “…clarified heart and liver homogenates were frozen, and subsequently pooled, depleted of hemoglobin using HemogloBind™ according to manufacturer’s instructions…prior to sucrose gradient fractionation. A second Biotech Support Group product, formerly called SeraFILE PROspector and now trademarked as NRicher™ 6, was used for sub-proteome enrichment. The article states “Affinity bead based sample pre-separations were performed forC. elegans lysates as per manufacturer’s instructions…fractions (SeraFILE bead eluates) were subjected to ion exchange fractionation…”. The authors conclude that many complexes are conserved across species, and by correlating the results with genome sequence information, are able to predict more than one million interactions in 122 eukaryotes.

    I am very pleased that two of our products were able to contribute to this rigorous examination of protein complexes. When our products were used as a pretreatment step in the overall workflow, about twice the number of observations and annotations became possible. This further validates that the sub-proteome bias characteristics of NRicher™ 6 can simplify complex proteomes into less complex sub-proteomes with efficiencies suitable for deep functional proteome characterization. Furthermore, this study demonstrated the importance of a key feature implicit to all of our products; that is the maintenance of functional and structural integrity after separations. Without that particular feature, these additional observations would not have been possible.” states Swapan Roy, Ph.D., President and Founder of Biotech Support Group.