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CANT1 Protein

Produkt-Information von CANT1 Protein

Synonym CANT1, SHAPY
Protein Construction

A DNA sequence encoding the human CANT1(Q8WVQ1-1)(Gly80-Ile401) was expressed ,with the fused Fc region of human IgG1 at the N-terminus.

Source Human
Expression Host Human Cells

QC Testing von CANT1 Protein

Purity > 90 % as determined by SDS-PAGE SDS-PAGE:
SDS-PAGE

CANT1 protein

Endotoxin < 1.0 EU per μg of the protein as determined by the LAL method
Stability Samples are stable for up to twelve months from date of receipt at -70℃
Predicted N terminal Glu
Molecular Mass

The recombinant human CANT1/Fc is a disulfide-linked homodimer. The reduced monomer comprises 582 amino acids and has a predicted molecular mass of 64.3 kDa. The apparent molecular mass of the protein is approximately 65 kDa in SDS-PAGE under reducing conditions due to glycosylation.

Formulation Lyophilized from a 0.2μm filtered solution of PBS, pH7.4.
  1. Normally 5 % - 8 % trehalose and mannitol are added as protectants before lyophilization. Specific concentrations are included in the hardcopy of COA.

Usage Guide von CANT1 Protein

Storage Store it under sterile conditions at -70℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
Reconstitution A hardcopy of COA with reconstitution instruction is sent along with the products. Please refer to it for detailed information.

Verwandte Produkte & Themen von CANT1 Protein

Related Areas:

Enzyme>>Other>> CANT1

Proteins:
Molecule Species Description //For Detailed Info. and Price------CLICK! Cat. No
CANT1 Human CANT1 Protein, Recombinant 13124-H01H
CANT1 Human CANT1 Protein, Recombinant 13124-H07H
Antibodies:

Beschreibung von CANT1 Protein

CANT1(calcium activated nucleotidase 1, N-Histidine-tagged) belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Alternatively spliced transcript variants have been noted for this gene. Defects in CANT1 are the cause of desbuquois dysplasia. A chondrodysplasia characterized by severe prenatal and postnatal growth retardation (less than -5 SD), joint laxity, short extremities, progressive scoliosis, round face, midface hypoplasia, prominent bulging eyes. The main radiologic features are short long bones with metaphyseal splay, a 'Swedish key' appearance of the proximal femur (exaggerated trochanter), and advance carpal and tarsal bone age. Two forms of desbuquois dysplasia are distinguished on the basis of the presence (type 1) or absence (type 2) of characteristic hand anomalies: an extra ossification center distal to the second metacarpal, delta phalanx, bifid distal thumb phalanx, and phalangeal dislocations.

References

  1. Failer BU. et al., 200, J Biol Chem. 277 (40): 36978-86.
  2. Smith TM et al., 2002, Arch Biochem Biophys. 406 (1): 105-15.
  3. Strausberg RL. et al., 2003, Proc Natl Acad Sci. 99 (26): 16899-903.

Sino Biological Inc. liefert CANT1 Protein mit höherer Qualität und günstiger Kosten im Vergleich mit anderen globalen Lieferanten.

Weitere Informationen über CANT1 Protein lesen Sie bitte: http://www.sinobiological.com/CANT1-Protein-g-9530.html

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