|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive, Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
A polyhistidine-tag is an amino acid motif in proteins that consists of at least five histidine (His) residues, often at the N- or C-terminus of the protein.
Polyhistidine-tags are often used for affinity purification of polyhistidine-tagged recombinant proteins expressed in Escherichia coli and other prokaryotic expression systems.
|Human CDH16 ORF mammalian expression plasmid, C-GFPSpark tag||HG10915-ACG|
|Human CDH16 ORF mammalian expression plasmid, C-OFPSpark / RFP tag||HG10915-ACR|
|Human CDH16 ORF mammalian expression plasmid, C-Flag tag||HG10915-CF|
|Human CDH16 ORF mammalian expression plasmid, C-His tag||HG10915-CH|
|Human CDH16 ORF mammalian expression plasmid, C-Myc tag||HG10915-CM|
|Human CDH16 ORF mammalian expression plasmid, C-HA tag||HG10915-CY|
|Human CDH16 Gene cDNA clone plasmid||HG10915-M|
|Human CDH16 ORF mammalian expression plasmid, Flag tag||HG10915-M-F|
|Human CDH16 ORF mammalian expression plasmid, N-Flag tag||HG10915-NF|
|Human CDH16 ORF mammalian expression plasmid, N-His tag||HG10915-NH|
|Human CDH16 ORF mammalian expression plasmid, N-Myc tag||HG10915-NM|
|Human CDH16 ORF mammalian expression plasmid, N-HA tag||HG10915-NY|
|Human CDH16 natural ORF mammalian expression plasmid||HG10915-UT|
|Learn more about expression Vectors|
KSP-Cadherin/Cadherin-16 is a member of the cadherin superfamily, calcium-dependent, membrane-associated glycoproteins. The protein consists of an extracellular domain containing 6 cadherin domains, a transmembrane region and a truncated cytoplasmic domain but lacks the prosequence and tripeptide HAV adhesion recognition sequence typical of most classical cadherins. Expression is exclusively in kidney, where the protein functions as the principal mediator of homotypic cellular recognition, playing a role in the morphogenic direction of tissue development. KSP-Cadherin/Cadherin-16 can be detected at later stages of tubulogenesis during human renal development and in the distal tubules of adult kidneys, no expression was found by immunohistochemistry or Western blot analysis in RCC tumour tissues and several RCC cell lines. However, despite the lack of protein expression, mRNA synthesis of KSP-Cadherin/Cadherin-16 could be detected by reverse transcriptase-polymerase chain reaction analysis in all RCC tissues and most of the RCC cell lines studied, although at a reduced level. The loss of KSP-Cadherin/Cadherin-16 protein was only observed in the malignant part of the tumour kidneys, whereas in the normal part of the affected kidneys KSP-Cadherin/Cadherin-16 expression was clearly detected. These results indicate a downregulation of Ksp-cadherin in RCC and suggest a role for this cell adhesion molecule in tumour suppression.