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Conditions of optimal HSPB8 Protein 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
HSPB8 displays temperature-dependent chaperone activity. HSPB8 acts as a mn(2+)-dependent serine-threonine- specific protein kinase. we are not convinced that this is its true role. Defects in HSPB8 are a cause of distal hereditary motor neuropathy type ii (DHMN2) also known as distal spinal muscular atrophy (DSMA) and spinal muscular atrophy of the charcot-marie-tooth type. it is an autosomal dominant disorder of lower motor neurons characterized by distal muscle weakness.
BP002307-HSP-022: Recombinant Human Heat Shock Protein 22 kDa Protein-8 (HSPB8)
Source: E. coli-derived.
Formulation: The HSPB8 protein was lyophilized from a concentrated (1 mg/ml) solution containing 20 mM Tris-acetate, pH-7.6, 10 mM NaCl, 0.1 mM EDTA, 0.1 mM PMSF, 15 mM Beta-ME.
Purity: > 95.0% as determined by SDS-PAGE.
Reconstitution: It is recommended to reconstitute the lyophilized HSPB8 in sterile 18 M?-cm H2O not less than 100 ug/ml, which can then be further diluted to other aqueous solutions.
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.
1 month, 2 to 8°C under sterile conditions after reconstitution.
3 months, -20 to -70°C under sterile conditions after reconstitution.
Other HSPB8 Proteins:
Recombinant Human Heat Shock Protein 22 kDa Protein-8, His Tag
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