|Datasheet||Specific References||Reviews||Related Products||Protocols|
|Vector Type||Mammalian Expression Vector|
|Expression Method||Constiutive, Stable / Transient|
|Selection In Mammalian Cells||Hygromycin|
Human influenza hemagglutinin (HA) is a surface glycoprotein required for the infectivity of the human virus. The HA tag is derived from the HA-molecule corresponding to amino acids 98-106 has been extensively used as a general epitope tag in expression vectors. Many recombinant proteins have been engineered to express the HA tag, which does not appear to interfere with the bioactivity or the biodistribution of the recombinant protein. This tag facilitates the detection, isolation, and purification of the proteins.
The actual HA tag is as follows: 5' TAC CCA TAC GAT GTT CCA GAT TAC GCT 3' or 5' TAT CCA TAT GAT GTT CCA GAT TAT GCT 3' The amino acid sequence is: YPYDVPDYA.
|Rat F9 ORF mammalian expression plasmid, C-GFPSpark tag||RG81664-ACG|
|Rat F9 ORF mammalian expression plasmid, C-OFPSpark / RFP tag||RG81664-ACR|
|Rat F9 ORF mammalian expression plasmid, C-Flag tag||RG81664-CF|
|Rat F9 ORF mammalian expression plasmid, C-His tag||RG81664-CH|
|Rat F9 ORF mammalian expression plasmid, C-Myc tag||RG81664-CM|
|Rat F9 ORF mammalian expression plasmid, C-HA tag||RG81664-CY|
|Rat F9 Gene cDNA clone plasmid||RG81664-G|
|Rat F9 ORF mammalian expression plasmid, N-Flag tag||RG81664-NF|
|Rat F9 ORF mammalian expression plasmid, N-His tag||RG81664-NH|
|Rat F9 ORF mammalian expression plasmid, N-Myc tag||RG81664-NM|
|Rat F9 ORF mammalian expression plasmid, N-HA tag||RG81664-NY|
|Rat F9 natural ORF mammalian expression plasmid||RG81664-UT|
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Coagulation factor IX, also known as Christmas factor, Plasma thromboplastin component and PTC, is a secreted protein which belongs to the peptidase S1 family. Coagulation factor IX / F9 contains two EGF-like domains, one Gla (gamma-carboxy-glutamate) domain and one?peptidase S1 domain. Coagulation factor IX / F9 is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca2+ons, phospholipids, and factor VIIIa. Defects in Coagulation factor IX / F9 are the cause of thrombophilia due to factor IX defect which is a hemostatic disorder characterized by a tendency to thrombosis. Defects in Coagulation factor IX / F9 are also the cause of recessive X-linked hemophilia B ( HEMB ) which also known as Christmas disease.