
Background
Cross-Reactive Material 197 (CRM197) is a genetically non-toxic form of diphtheria toxin (DT). A single base change (glutamic acid to glycine at position 52) in CRM197 disables the ADP-ribosylation activity of the A chain attenuating toxicity1, 2. Although CRM197 is non-toxic, it is immunologically indistinguishable from diphtheria toxin. CRM197 functions as a carrier for polysaccharides and haptens making them immunogenic in a number of conjugate vaccines.
Scarab Genomics’ CRM197 is a recombinant form expressed in Clean Genome® E. coli, our proprietary platform.
SOURCEClean Genome® E. coli expressed recombinant CRM197
PRODUCT MOLECULAR MASS: 58.4 kDa
Figures
Figure 1: Scarab Genomics’ CRM197 is exceptionally pure and consistent from lot to lot. Five replicates of each lot of Scarab’s CRM197 were run on a Bis-Tris 4-12% gradient SDS polyacrylamide gel and stained with GelCode™ Blue, then purity assessed via gel scan. The average purity for each lot was calculated and assigned as follows: Panel A 98.3% pure, Panel B 95.5% pure.

Figure 2: Scarab Genomics’ CRM197 is higher purity than other commercially available sources. Two micrograms of CRM197 from each source were run on a Bis-Tris 4-12% gradient SDS polyacrylamide gel and stained with GelCode™ Blue. Breakdown products (indicated as bands A and B), are virtually absent in the Scarab product. Smeared background in some lanes is due to protein degradation and carry-over of host proteins, both are minimal in the Scarab product. Lane 1 Size Marker, Lane 2 empty Lane 3 Scarab Genomics CRM197,SG1 Lane 4 Scarab Genomics CRM197, SG2, Lane 5 vendor F, Lane 6 vendor M, and Lane 7 vendor L.

Figure 3: LC MS peptide mapping of Scarab’s CRM197 confirms it is biosimilar to native CRM197. Amino acid sequencing and mass spectrometry (MS) on were performed on Scarab’s highly pure CRM197. Extensive bioinformatics analysis of MS material revealed no post-translational modifications. Trypsin and chymotrypsin digestion followed by nano-liquid chromatography-MS/MS identified very high protein coverage (~97-98%). Electrospray ionization mass spectrometry (ESI-MS) on Scarab CRM197 confirmed the expected peptide sequence. Neither differences to the reported amino acid composition nor side chain modifications were observed.

Figure 4: Scarab’s CRM197 conjugates as effectively. Not all lysines in CRM197 are exposed on the protein surface for potential conjugation. Employing Solulink’s ChromaLink™ Biotin conjugation assays (San Diego, CA), which utilize a NHS ester reaction scheme to conjugate Biotin to primary amines, we confirmed at least 10 sites on Scarab’s CRM197 are accessible for conjugation. This optically quantitative (absorbance at 354 nm) functional test confirms the lysines on Scarab’s CRM197 are accessible for conjugation with hapten, like native CRM197.
Specifications
Quality Control
Purity: |
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| |
Concentration: | 4 mg/mL in 150mM NaCl, 25mM HEPES, pH7.4 via absorbance at 280 nm using an E0.1%=1.07 for a 1 mg/mL solution |
Endotoxin: | ≤25 EU/mg of protein by the kinetic turbidimetric LAL method (maximum sensitivity = 0.01 EU/mL) |
Dimer: | ≤5% |
Grade: CRM197 is for Research Use Only, Not for use in humans or as a diagnostic agent.
Storage Conditions:
- CRM197 is a 0.2 μm-filtered frozen solution of 4 mg/mL CRM197, 150mM NaCl, 25mM HEPES, pH 7.4. Store at -70°C upon receipt.
- To minimize aggregation, thaw CRM197 in 37°C water bath for 1 hour.
- Repeated freeze-thaw cycles can degrade material. To minimize freeze-thaw cycles, aliquot CRM197 to match desired use.
- Handle product gently, DO NOT VORTEX.
Related Products
Support
Product ManualsScarab Genomics CRM197 Liquid Data SheetPosters
- Economic QBD Production of the Conjugate Vaccine Carrier Protein, CRM197 by a Continuous Manufacturing Process Using Scarab Genomics’ Clean Genome® E. coli
- Scarab Genomics Proprietary Platform for Continuous Manufacturing of Pharmaceutical Biologics Applied to CRM197
- Giannini, G., Rappuoli, R., and Ratti, G. (1984) Nucleic Acids Research, 12 (10):4063-4069.
- Mekada, E., and Uchida, T. (1985) Journal of Biological Chemistry, 260:12148-12153.
Patents & Disclaimers
Scarab is providing you with this Material subject to the non-transferable right to use the subject amount of the Material for your research at your academic institution. The Recipient agrees not to sell or otherwise transfer this Material, or anything derived or produced from the Material to a third party. NO RIGHTS ARE PROVIDED TO USE THE MATERIAL OR ANYTHING DERIVED OR PRODUCED FROM THE MATERIAL FOR COMMERCIAL PURPOSES. If the Recipient makes any changes to the chromosome of the Material that results in an invention in breach of this limited license, then Scarab will have a worldwide, exclusive, royalty-free license to such invention whether patentable or not. If the Recipient is not willing to accept the terms of this limited license, Scarab is willing to accept return of this product with a full refund, minus shipping and handling costs. For information on obtaining a license to this Material for purposes other than research, please contact Scarab’s Licensing Department. Scarab Genomics’ technology is covered by the following Patent Applications: US, 15/122,891, PCT/US2016/25588 and their related foreign applications.Clean Genome® is a registered trademark of Scarab Genomics, LLC.
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2-IgM也是一种特异性感染指标,但在人体内持续时间不长(有时是30天更短),往往是传染病的近期感染指标。呈阴性是指:你近期没有感染过结核杆菌。
您好,对于优生学检查,有两种抗体,一种是IGG抗体,一种是IGM抗体,如果是前者阳性,只能说明即往以前有感染了这类病原体,而不能说明当前正在感染这个病毒的。
指导意见:
如果是后一种阳性,也就是说IGM抗体阳性时,就提示当前正在感染这个病毒的,需要及时行抗病毒的药物治疗为佳,治好后才行怀孕的,否则对于怀孕的胎儿有很大的影响的。
aware可自测不用抽血祝您健康天 猫!
IgM是免疫球蛋白M(Immunoglobulin M,IgM)的缩写。根据结构的不同将免疫球蛋白分为五种,IgM是人的免疫球蛋白之一,其他还有lgA、lgG、IgD和lgE。
文章原文链接http://www.jbc.org/content/282/23/16776.long
1,IgG抗体是抗体中分子量最小的一种,可通过胎盘输给胎儿,保护了婴儿最初六个月内免受感染。该抗体产生晚,维持时间长,消失慢,浓度高。血中检测到可作为远期感染指标。
2,IgM抗体是抗体中分子量最大的一种,不能通过胎盘输给胎儿。抗体产生最早,一经感染,快速产生,在感染初期抗感染起作用。但维持时间短,消失快。
3,灵长类动物主要有四种免疫球蛋白IgG、IgM、IgA、和IgE。
所有用于检测抗原的免疫学方法经适当改良后,均可用于抗体的检测,如IFA、ELISA、RIA、LA......由于抗原方法的敏感性提高和PCR技术的应用,使得HSV抗体在HSV感染个体中的不均一性和不稳定性影响了这类指标在临床诊断中的意义,但作为一种感染有关指标,在一定的范围和情况下,仍有必要进行检测和深入研究.目前HSV特异性抗体的检测,主要有IgG、IgM和IgA三种。

