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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.
|Human RNASET2 Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG13509-G-F|
|Human RNASET2 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG13509-G-H|
|Human RNASET2 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG13509-G-M|
|Human RNASET2 Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG13509-G-N|
|Human RNASET2 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG13509-G-Y|
RNASET2 (ribonuclease T2) is an enzyme which belongs to the RNase T2 family. It is highly expressed in the temporal lobe and fetal brain. RNASET2 gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular ribonucleases. It is a single copy gene that maps to 6q27, a region associated with human malignancies and chromosomal rearrangement. Defects in RNASET2 are the cause of leukoencephalopathy cystic without megalencephaly. An infantile-onset syndrome of cerebral leukoencephalopathy. Affected newborns develop microcephaly and neurologic abnormalities including psychomotor impairment, seizures and sensorineural hearing impairment. The brain shows multifocal white matter lesions, anterior temporal lobe subcortical cysts, pericystic abnormal myelination, ventriculomegaly and intracranial calcifications.