|Datasheet||Specific References||Reviews||Related Products||Protocols|
|ORF Clone of Homo sapiens pancreatic lipase-related protein 1 DNA.|
|Identical with the Gene Bank Ref. ID sequence.|
|Whatman FTA elute card (Cat: WB120410) contains 5-10 μg of plasmid.|
|The Whatman FTA elute card can be stored at room temperature for three months under dry condition.|
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 PNLIPRP1 Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG13565-G-F|
|Human PNLIPRP1 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG13565-G-H|
|Human PNLIPRP1 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG13565-G-M|
|Human PNLIPRP1 Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG13565-G-N|
|Human PNLIPRP1 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG13565-G-Y|
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PNLIPRP1, also known as PLRP1, belongs to the AB hydrolase superfamily, Lipase family. PNLIPRP1 is structurally similar to PLRP2. However, these two proteins display different functional properties. PNLIPRP1 may function as inhibitor of dietary triglyceride digestion. It lacks detectable lipase activity towards triglycerides, diglycerides, phosphatidylcholine, galactolipids or cholesterol esters. PLRP2 hydrolyses milk fat with a lower catalytic efficiency than that of PL. PLRP2 activity, higher on homogenized than on native milk fat, is differently influenced by fatty acids and colipase depending on a proteolytic cleavage in the lid domain.