|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.
|Mouse ATL1 ORF mammalian expression plasmid, C-GFPSpark tag||MG50784-ACG|
|Mouse ATL1 ORF mammalian expression plasmid, C-OFPSpark / RFP tag||MG50784-ACR|
|Mouse ATL1 ORF mammalian expression plasmid, C-Flag tag||MG50784-CF|
|Mouse ATL1 ORF mammalian expression plasmid, C-His tag||MG50784-CH|
|Mouse ATL1 ORF mammalian expression plasmid, C-Myc tag||MG50784-CM|
|Mouse ATL1 ORF mammalian expression plasmid, C-HA tag||MG50784-CY|
|Mouse ATL1 Gene cDNA clone plasmid||MG50784-G|
|Mouse ATL1 ORF mammalian expression plasmid, N-Flag tag||MG50784-NF|
|Mouse ATL1 ORF mammalian expression plasmid, N-His tag||MG50784-NH|
|Mouse ATL1 ORF mammalian expression plasmid, N-Myc tag||MG50784-NM|
|Mouse ATL1 ORF mammalian expression plasmid, N-HA tag||MG50784-NY|
|Mouse ATL1 natural ORF mammalian expression plasmid||MG50784-UT|
|Learn more about expression Vectors|
Atlastin-1, also known as Spastic paraplegia 3 protein A, Guanine nucleotide-binding protein 3, GTP-binding protein 3, GBP3, ATL1 and SPG3A, is a multi-pass membrane protein which belongs to the GBP family and atlastin subfamily. ATL1 / SPG3A is expressed predominantly in the adult and fetal central nervous system. Expression of ATL1 / SPG3A in adult brain is at least 50-fold higher than in other tissues. ATL1 / SPG3A is detected predominantly in pyramidal neurons in the cerebral cortex and the hippocampus of the brain. ATL1 / SPG3A is also expressed in upper and lower motor neurons (at protein level). A distinguishing feature of ATL1 / SPG3A is its frequent early onset, raising the possibility that developmental abnormalities may be involved in its pathogenesis. Missense SPG3A mutant atlastin-1 proteins have impaired GTPase activity and may act in a dominant-negative, loss-of-function manner by forming mixed oligomers with wild-type atlastin-1. Defects in ATL1 / SPG3A are the cause of spastic paraplegia autosomal dominant type 3 (SPG3), also known as Strumpell-Lorrain syndrome. Spastic paraplegia is a degenerative spinal cord disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs.