| Code | CSB-YP331130DZQ |
| MSDS | |
| Size | Pls inquire |
| Source | Yeast |
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| Code | CSB-EP331130DZQ |
| MSDS | |
| Size | Pls inquire |
| Source | E.coli |
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| Code | CSB-EP331130DZQ-B |
| MSDS | |
| Size | Pls inquire |
| Source | E.coli |
| Conjugate | Avi-tag Biotinylated E. coli biotin ligase (BirA) is highly specific in covalently attaching biotin to the 15 amino acid AviTag peptide. This recombinant protein was biotinylated in vivo by AviTag-BirA technology, which method is BriA catalyzes amide linkage between the biotin and the specific lysine of the AviTag. |
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| Code | CSB-BP331130DZQ |
| MSDS | |
| Size | Pls inquire |
| Source | Baculovirus |
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| Code | CSB-MP331130DZQ |
| MSDS | |
| Size | Pls inquire |
| Source | Mammalian cell |
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This recombinant Cupriavidus necator Protein CbxX, chromosomal (cbxXC) is a semi-custom product. There are 5 expression system options: Yeast, E. coli, In Vivo Biotinylation in E. coli, Baculovirus, and Mammalian cell. Your requirements will be given top priority in determining the protein tags. For proteins within 800 aa, risk-free custom service is guaranteed. It means you will not be charged if the protein cannot be delivered.
Cupriavidus necator CbxXC protein is a crucial component involved in the biosynthesis of polyhydroxybutyrate (PHB) in Cupriavidus necator. This bacterium, previously known as Ralstonia eutropha or Alcaligenes eutrophus, is renowned for its ability to accumulate PHB, with levels reaching 80% to 90% of its dry cell weight under specific growth conditions [1][2]. Cupriavidus necator is a Gram-negative β-proteobacterium with a versatile genome comprising four replicons and over 6000 protein-coding genes [3]. The bacterium produces PHB using various carbon sources, including fructose, glucose, alcohols, amino acids, and CO2-H2 mixtures [4].
References:
[1] C. Chien, H. Li, P. Soo, S. Chen, Y. Wei, & W. Chen, Effects of different substrate composition on biosynthesis of polyhydroxybutyrate-co-hydroxyvalerate by recombinant escherichia coli, Applied Biochemistry and Biotechnology, vol. 166, no. 3, p. 796-804, 2011. https://doi.org/10.1007/s12010-011-9469-7
[2] S. Obruča, I. Márová, Z. Svoboda, & R. Mikulíková, Use of controlled exogenous stress for improvement of poly(3-hydroxybutyrate) production in cupriavidus necator, Folia Microbiologica, vol. 55, no. 1, p. 17-22, 2010. https://doi.org/10.1007/s12223-010-0003-z
[3] A. Lykidis, D. Pérez‐Pantoja, T. Ledger, K. Mavromatis, I. Anderson, N. Ivanovaet al., The complete multipartite genome sequence of cupriavidus necator jmp134, a versatile pollutant degrader, Plos One, vol. 5, no. 3, p. e9729, 2010. https://doi.org/10.1371/journal.pone.0009729
[4] J. Panich, B. Fong, & S. Singer, Metabolic engineering of cupriavidus necator h16 for sustainable biofuels from co2, Trends in Biotechnology, vol. 39, no. 4, p. 412-424, 2021. https://doi.org/10.1016/j.tibtech.2021.01.001
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KEGG: reh:H16_B1393
STRING: 381666.H16_B1393