![ICC/IF analysis of 4%PFA-fixed NIH-3T3 using GTX03698 ATP7b antibody [S62-29]. Green : Primary antibody Blue : DAPI Red : F-Actin Dilution : 1:100 ICC/IF analysis of 4%PFA-fixed NIH-3T3 using GTX03698 ATP7b antibody [S62-29]. Green : Primary antibody Blue : DAPI Red : F-Actin Dilution : 1:100](https://www.genetex.com/upload/website/prouct_img/normal/GTX03698/GTX03698_20220518_ICCIF_1_w_23053123_518.webp)
ICC/IF analysis of 4%PFA-fixed NIH-3T3 using GTX03698 ATP7b antibody [S62-29]. Green : Primary antibody Blue : DAPI Red : F-Actin Dilution : 1:100
ATP7b antibody [S62-29]
GTX03698
ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
Product group Antibodies
ReactivityHuman, Mouse, Rat
TargetATP7B
Overview
- SupplierGeneTex
- Product NameATP7b antibody [S62-29]
- Delivery Days Customer9
- Application Supplier NoteWB: 1:1000. ICC/IF: 1:100. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, ImmunoPrecipitation, Western Blot, ImmunoCytoChemistry, ImmunoHistoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDS62-29
- Concentration1 mg/ml
- ConjugateUnconjugated
- Gene ID540
- Target nameATP7B
- Target descriptionATPase copper transporting beta
- Target synonymsATPase, Cu(2+)- transporting, beta polypeptide; ATPase, Cu++ transporting, beta polypeptide; copper pump 2; copper-transporting ATPase 2; copper-transporting protein ATP7B; PWD; WC1; WD; Wilson disease-associated protein; WND
- HostMouse
- IsotypeIgG1
- Protein IDP35670
- Protein NameCopper-transporting ATPase 2
- Scientific DescriptionThis gene is a member of the P-type cation transport ATPase family and encodes a protein with several membrane-spanning domains, an ATPase consensus sequence, a hinge domain, a phosphorylation site, and at least 2 putative copper-binding sites. This protein functions as a monomer, exporting copper out of the cells, such as the efflux of hepatic copper into the bile. Alternate transcriptional splice variants, encoding different isoforms with distinct cellular localizations, have been characterized. Mutations in this gene have been associated with Wilson disease (WD). [provided by RefSeq, Jul 2008]
- ReactivityHuman, Mouse, Rat
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203