
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: |
|
| |
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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我现在做关于细胞膜分子交联,然后用western检测多聚体的实验
遇到很大的困难
刚开始用真核细胞做,就发现细胞交联后提取蛋白,比未交联的细胞蛋白总量减少
后来用原核先提取蛋白做实验
发现交联终止后,做western交联的孔曝光没有条带,后来用同样的方法重新做了一次PAGE,染胶,发现蛋白不见了
为什么交联后蛋白减少或是不见了呢
我用的都是Pierce公司的交联剂,用过EGS和BOSCOES,都有同样的问题
方法是综合说明书和一片文献上来的
到底问题出在哪里呢
请各位大侠帮帮忙
实验卡在这里进行不下去了
我快急死了
请有经验的,用过交联剂的老师,同学多多指导
万分感谢!!
指在光、热、高能辐射、机械力、超声波和交联剂等作用下,大分子链间通过化学键联结起来,形成网状或体形结构高分子的过程。橡胶的硫化、不饱和树脂的交联、环氧树脂的熟化等都是化学交联的例子。通过化学交联可改善聚合物的性能。如聚乙烯的化学交联可提高其强度和耐热性,又如皮革的鞣制过程是利用其蛋白质分子与甲醛作用,生成交联桥,以至失去溶解性。
明胶与干酪素都是蛋白质类,其分子结构同属氨基酸,但前者比后者价格便宜很多,而且在我国的产盆很大,因此具有代替干酪素做涂料胶粘剂的可能性。
在许多的细胞生命活动中,例如DNA复制、mRNA转录与修饰以及病毒的感染等都涉及到DNA与蛋白质之间的相互作用的问题.
重组DNA技术的发展,人们已分离到了许多重要的基因.现在的关键问题是需要揭示环境因子及发育信号究竟是如何控制基因的转录活性.为此需要:
a、鉴定分析参与基因表达调控的DNA元件;
b、分离并鉴定这些顺式元件特异性结合的蛋白质因子;
这些问题的研究都涉及到DNA与蛋白质之间的相互作用.
研究DNA-蛋白质相互作用的实验方法主要包括:
a、凝胶阻滞实验; b、DNase 1 足迹实验;
c、甲基化干扰实验; d、体内足迹实验; f、拉下实验.

