( We provide with CANT1 qPCR primers for gene expression analysis, HP101975 )
The pGEM-T is 3kb in length, and contains the amplicin resistance gene, conferring selection of the plasmid in E. coli, and the ori site which is the bacterial origin of replication. The plasmid has multiple cloning sites as shown below. The coding sequence was inserted by TA cloning. Many E. coli strains are suitable for the propagation of this vector including JM109, DH5α and TOP10.
The coding sequence can be easily obtained by digesting the vector with proper restriction enzyme(s). The coding sequence can also be amplified by PCR with M13 primers, or primer pair SP6 and T7.
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-GFPSpark 标签||HG13266-ACG|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-OFPSpark 标签||HG13266-ACR|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-Flag 标签||HG13266-CF|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-His 标签||HG13266-CH|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-Myc 标签||HG13266-CM|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), C-HA 标签||HG13266-CY|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), N-Flag 标签||HG13266-NF|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), N-His 标签||HG13266-NH|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), N-Myc 标签||HG13266-NM|
|人 CANT1 基因ORF全长cDNA克隆(表达载体), N-HA 标签||HG13266-NY|
|人 CANT1 基因ORF全长cDNA克隆(表达载体)||HG13266-UT|
CANT1(calcium activated nucleotidase 1) belongs to the apyrase family. Apyrase is a calcium-activated plasma membrane-bound enzyme (magnesium can also activate it) (EC 126.96.36.199) that catalyses the hydrolysis of ATP to yield AMP and inorganic phosphate. Two isoenzymes are found in commercial preparations from S. tuberosum. One with a higher ratio of substrate selectivity for ATP: ADP and another with no selectivity. It can also act on ADP and other nucleoside triphosphates and diphosphates with the general reaction being NTP -> NDP + Pi -> NMP + 2Pi. The salivary apyrases of blood-feeding arthropods are nucleotide hydrolysing enzymes are implicated in the inhibition of host platelet aggregation through the hydrolysis of extracellular adenosine diphosphate. CANT1 functions as a calcium-dependent nucleotidase with a preference for UDP. Defects in CANT1 are the cause of desbuquois dysplasia.