SKU: WP11091 Categories: ,

AQP0 Polyclonal Antibody

Price range: $268.00 through $328.00

SKU: WP11091-100
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Product details

Background:

Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. The function of the fiber cell membrane protein encoded by this gene is undetermined, yet this protein is speculated to play a role in intracellular communication. The MIP protein is expressed in the ocular lens and is required for correct lens function. This gene has been mapped among aquaporins AQP2, AQP5, and AQP6, in a potential gene cluster at 12q13. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetAQP0
ReactivityHuman, Mouse, Rat
ApplicationsWB, IHC, IF, ELISA
MW(Calculated)
MW(Observed)28kD
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; IHC 1:100-1:300; ELISA 1:5000; IF 1:50-200 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenThe antiserum was produced against synthesized peptide derived from human AQP0. AA range:95-144
SpecificityAQP0 Polyclonal Antibody detects endogenous levels of AQP0 protein.
Gene NameMIP
Protein NameLens fiber major intrinsic protein
Other NameMIP; / AQP0; / Lens fiber major intrinsic protein; / Aquaporin-0; / MIP26; / MP26
SpeciesHuman
Gene ID4284
UniprotP30301,
Species.1Mouse
Gene ID.117339
Uniprot.1P51180,
Species.2Rat
Gene ID.2
Uniprot.2P09011
Cellular LocalizationCell membrane; Multi-pass membrane protein . Cell junction, gap junction .
Tissue ExpressionExpressed in the cortex and nucleus of the retina lens (at protein level) (PubMed:30790544). Major component of lens fiber gap junctions (PubMed:24120416).
Signaling_pathway
Research Areas
FunctionDisease:Defects in MIP are a cause of autosomal recessive congenital cataract [MIM:154050].,Domain:Aquaporins contain two tandem repeats each containing three membrane-spanning domains and a pore-forming loop with the signature motif Asn-Pro-Ala (NPA).,Function:Water channel. May be responsible for regulating the osmolarity of the lens.,similarity:Belongs to the MIP/aquaporin (TC 1.A.8) family.,tissue specificity:Major component of lens fiber gap junctions.,
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