|Datasheet||Specific References||Reviews||Related Products||Protocols|
|ORF Clone of Homo sapiens mitogen-activated protein kinase 8, transcript variant JNK1-b2 DNA.|
|JNK, JNK1, PRKM8, SAPK1, JNK1A2, JNK21B1/2|
|pMD18-T Simple Vector|
|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.|
pMD18-T Simple Vector is a high-efficiency TA cloning vector constructed from pUC18, of which the initial multiple cloning sites (MCS) were destroyed. Thus the cDNA should be amplified by PCR with primers containing a restriction site for subclone. Competent cells appropriate for pUC18 are also appropriated for the Vector, e.g. JM109, DH5α, TOP10. The pMD18-T Simple Vector is 2.6kb in size. Selection of the plasmid in E. coli is conferred by the ampicillin resistance gene. The coding sequence was inserted by TA cloning at site 425.
The coding sequence can be amplified by PCR with M13-47 and RV-M primers.
|Human MAPK8 transcript variant JNK1-b2 Gene cDNA Clone (full-length ORF Clone), expression ready, FLAG-tagged||HG10795-M-F|
|Human MAPK8 transcript variant JNK1-b2 Gene cDNA Clone (full-length ORF Clone), expression ready, His-tagged||HG10795-M-H|
|Human MAPK8 transcript variant JNK1-b2 Gene cDNA Clone (full-length ORF Clone), expression ready, Myc-tagged||HG10795-M-M|
|Human MAPK8 transcript variant JNK1-b2 Gene cDNA Clone (full-length ORF Clone), expression ready, untagged||HG10795-M-N|
|Human MAPK8 transcript variant JNK1-b2 Gene cDNA Clone (full-length ORF Clone), expression ready, HA-tagged||HG10795-M-Y|
|Product name||Product name|
Mitogen-activated protein kinase 8 (MAPK8), also known as JNK1, is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. The protein kinases JNK1 has been found to serve as critical molecular links between obesity, metabolic inflammation, and disorders of glucose homeostasis. It is critically involved in the promotion of diet-induced obesity, metabolic inflammation, insulin resistance, and beta-cell dysfunction. The selective deficiency of JNK1 in the murine nervous system is sufficient to suppress diet-induced obesity. JNK1 is also implicated in the mechanism of obesity-induced insulin resistance. Genetic analysis indicates that the effects of JNK1 on insulin resistance can be separated from effects of JNK1 on obesity. Emerging research indicates that JNK1 plays multiple roles in the regulation of insulin resistance, including altered gene expression, hormone/cytokine production, and lipid metabolism. JNK1 is a potential pharmacological target for the development of drugs that might be useful for the treatment of insulin resistance, metabolic syndrome, and type 2 diabetes. Furthermore, JNK1 plays a major role in the hypoxic cellular damage. JNK1 protein might be an attractive target for antihypoxic therapy in increasing resistance to many pathological conditions and diseases, leading to the oxygen deficit.