Technical Data
C1050
L-Canavanine Sulfate
1g
Biochemicals Storage: 4CShipping: RT
Canavanine, nitric oxide synthase inhibitor, is an analog of arginine. Both are imported into the cell via the same high-affinity permease, which is encoded by the can1 locus. High-level resistance to canavanine occurs exclusively because of mutation at this locus, but low-level resistance can arise at a number of other loci.

Because canavinine is a competitive inhibitor, arginine must be excluded from media used for testing sensitivity to the drug. Canavanine resistance must also be scored under high-nitrogen conditions, such as those provided by SD or SC medium, since the CAN1 permease will then provide the only entry route to the cell for arginine and canavanine. In the presence of low-nitrogen conditions, effectively those provided by YPD medium, the general amino acid permease (GAP) system is induced and arginine and canavanine can also be taken up by this route. In addition, Can r Arg-auxotrophs are viable on YPD but are inviable on synthetic media because they are unable to take up arginine.

Synonyms:
Canavalia ensiformis; O-Guanidino-L-homoserine, L- -Amino- -(guanidinooxy)-n-butyric acid sulfate

Purity (TLC):
98%

Appearance:
White, crystalline powder

Solubility (100mg/ml, H2O): Colorless, clear, complete

Water (KF):
As reported

Elemental Analysis:
Carbon, Nitrogen: As reported

Stock Solution:
Prepare 100mg/ml in molecular biology grade dH2O. Filter sterilize (0.2um).

Working Solution:
60mg/L is typically used in autoclaved SD- or SC- arg medium for scoring and selecting canavanine resistance.

Storage:
Lyophilized powder may be stored at 4C.

CAS Number:
2219-31-0

Molecular Formula:
C5H12N4O3 H2SO4

Molecular Weight:
274.25
Purity: ~98% (TLC)

Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
1. Kaiser, C., et al., Methods in Yeast Genetics, Cold Spring Harbor Laboratory Course Manual, A:216 (1994). 2. McCall, T.B., et al., Biochem. J. 261: 293 (1989). 3. Dokita, S., et al., Eur. J. Pharmacol. 266: 269 (1994). 4. Merck 12: 1783. 5. Knowles, et al., Biochem. J., 298: 249 (1994). 6. Dokita, et al., Eur. J. Pharm., 269: 269 (1994).

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.