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Bactenecin, bovine

Cat. No. Size Price Figures
RP11235-1 mg
 		1 mg
$ 57.00
MS:  20081201031120  (PDF)
HPLC:  20081201031151  (PDF)
MSDS:  20080702220412  (PDF)

STRUCTURE:
Bactenecin structure
Zoom

References:
  • Huang LC, et al. Multifunctional Roles of Human Cathelicidin (LL-37) at the Ocular Surface. Invest. Ophthalmol. Vis. Sci. Jun 2006; 47(6): 2369-2380.
  • Bergen PJ, et al. Colistin methanesulfonate is an inactive prodrug of colistin against Pseudomonas aeruginosa. Antimicrob. Agents Chemother. Jun 2006; 50(6): 1953-1958.
  • Lau YE, et al. Apoptosis of airway epithelial cells: human serum sensitive induction by the cathelicidin LL-37. Am. J. Respir. Cell Mol. Biol. Apr 2006; 34(4): 399-409.
RP11235-5 mg
 		5 mg
$ 228.00
Full Name
Bactenecin, bovine
Sequence
(one-letter code)		 RLCRIVVIRVCR
Sequence
(three-letter code)		{ARG}{LEU}{CYS}{ARG}{ILE}{VAL}{VAL}{ILE}{ARG}{VAL}
{CYS}{ARG}
Chemical BridgeDisulfide bridge: Cys3-Cys11
DescriptionBactenecin is an antimicrobial peptide isolated from bovine neutrophils. Bactenecin is synthesized by solid-phase peptide synthesis and renatured to a fully disulfide-bonded form. The peptide inhibits the growth of Escherichia coli and Staphylococcus aureus at the same concentration reported for the peptide purified from bovine neutrophils. Bactenecin inhibits the growth of other medically important bacteria and yeast, and it kills the fungus Trichophyton rubrum. Acetylation and amidation of the amino- and carboxy-termini of bactenecin do not change its potency, while replacement of its two cysteine residues with serine decreases potency.
FormulaC63H118N24O13S2
M.W.1483.9
Cas116229-36-8
Purity> 95%
StorageStore the peptide at -20°C. Keep container tightly closed.
* For Non-Clinical Research Use Only *
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