Recombinant Human Aquaporin-4(AQP4),partial CSB-EP001964HU
Specifications
| 20ug / 100ug / 1mg price = 100ug |
Alternative Name(s):
Mercurial-insensitive water channel ;MIWCWCH4
Species: (Organism)
Homo sapiens (Human)
Gene Names:
AQP4
Tag info:
N-terminal 6xHis-SUMO-tagged
Target Protein AA Sequence:
CPDVEFKRRFKEAFSKAAQQTKGSYMEVEDNRSQVETDDLILKPGVVHVIDVDRGEEKKGKDQSGEVLSSV
Expression Region:
253-323aa
Subcellular Location:
Membrane, Multi-pass membrane protein
Tissue Specificity:
Brain - muscle >> heart, kidney, lung, and trachea.
Protein Length:
Partial
Pathway:
Mol. Weight:
24 kDa
Purity:
Greater than 90% as determined by SDS-PAGE.
Form:
Liquid or Lyophilized powder
Buffer:
If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol. If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, pH 8.0.
Research Areas:
Transport
Function:
Forms a water-specific channel. Osmoreceptor which regulates body water balance and mediates water flow within the central nervous system.
Involvement in disease:
Relevance:
Forms a water-specific channel. Osmoreceptor which regulates body water balance and mediates water flow within the central nervous syst.
Reconstitution:
We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20℃/-80℃. Our default final concentration of glycerol is 50%. Customers could use it as reference.
Protein Families:
MIP/aquaporin (TC 1.A.8) family
Reference:
Megalencephalic leukoencephalopathy with subcortical cysts protein 1 functionally cooperates with the TRPV4 cation channel to activate the response of astrocytes to osmotic stress dysregulation by pathological mutations.Lanciotti A., Brignone M.S., Molinari P., Visentin S., De Nuccio C., Macchia G., Aiello C., Bertini E., Aloisi F., Petrucci T.C., Ambrosini E.Hum. Mol. Genet. 21:2166-2180(2012)
