Technical Data
CSTB (Cystatin-B, CPI-B, Liver Thiol Proteinase Inhibitor, Stefin-B, CST6, STFB) (FITC)
Component of the ubiquinol-cytochrome c reductase complex (complex III or cytochrome b-c1 complex), which is a respiratory chain that generates an electrochemical potential coupled to ATP synthesis.

Suitable for use in FLISA and Western Blot. Other applications not tested.

Recommended Dilution:
Optimal dilutions to be determined by the researcher.

Storage and Stability:
May be stored at 4C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot and store at -20C. Aliquots are stable for 12 months at -20C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. FITC conjugates are sensitive to light.
100ug-20CBlue IceHumanRabbit
As reported
Recombinant corresponding to human CSTB.
Purified by ammonium sulfate precipitation.
Supplied as a liquid in 0.01M PBS, PH 7.4, 0.03% Proclin 300, 50% glycerol. Labeled with fluorescein isothiocyanate (FITC).
Recognizes human CSTB.
Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.
1. "Mitochondrial genome diversity of native Americans supports a single early entry of founder populations into America." Silva W.A. Jr., Bonatto S.L., Holanda A.J., Ribeiro-Dos-Santos A.K., Paixao B.M., Goldman G.H., Abe-Sandes K., Rodriguez-Delfin L., Barbosa M., Paco-Larson M.L., Petzl-Erler M.L., Valente V., Santos S.E., Zago M.A. Am. J. Hum. Genet. 71:187-192 (2002). 2. "Serendipitous cloning of a mitochondrial cDNA and its polymorphism." Spurr N.K., Bodmer W.F. Mol. Biol. Med. 2:239-249 (1984). 3. "Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene." Keightley J.A., Anitori R., Burton M.D., Quan F., Buist N.R.M., Kennaway N.G. Am. J. Hum. Genet. 67:1400-1410 (2000).