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Conditions of optimal CA8 Enzyme performance should be determined experimentally by the investigator.
Price/availability/specifications subject to change without notice. Unless otherwise indicated, our catalog and customized products are for research use only and not intended for human or animal diagnostic or therapeutic use.
Phone: 1-617-401-8149
Fax: 1-617-606-5019
Email: message@sydlabs.com
Or leave a message with a formal purchase
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Introduction
Carbonic Anhydrase 8 (CA8) belongs to the alpha-carbonic anhydrase family. Alpha-carbonic anhydrase is a large family of zinc metalloenzymes that catalyze the reversible hydration of carbon dioxide. Because CA8 has some sequence similarity with other known carbonic anhydrase genes, it was firstly called as CA-related protein. Nevertheless, CA8 does not have a carbonic anhydrase catalytic activity. Defects in CA8 are the cause of cerebellar ataxia mental retardation and dysequilibrium syndrome type 3 (CMARQ3), which is a congenital cerebellar ataxia associated with dysarthia, quadrupedal gait and mild mental retardation.
BP001620-ENZ-235: Recombinant Human Carbonic Anhydrase 8 (CA8) Enzyme
Source: E. coli-derived.
A single, non-glycosylated polypeptide chain containing 314 amino acids (1-290) and having a molecular mass of 35.5 kDa. CA8 is fused to a 24 amino acid His-tag at N-terminus.
Purity: > 90% by SDS-PAGE.
Formulation: The CA8 solution (1 ug/ml) contains 20 mM Tris-HCl buffer (pH 8.0), 1 mM DTT and 20% glycerol.
Shipping: The product is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage: Use a manual defrost freezer and avoid repeated freeze-thaw cycles. 12 months from date of receipt, -20 to -70°C as supplied
Other CA8 Enzymes:
Recombinant Human CA8 Enzyme
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