![WB analysis of various samples using GTX03239 PER3 antibody [GT1327]. Dilution : 1:1000 Loading : 25microg per lane WB analysis of various samples using GTX03239 PER3 antibody [GT1327]. Dilution : 1:1000 Loading : 25microg per lane](https://www.genetex.com/upload/website/prouct_img/normal/GTX03239/GTX03239_18_WB_w_23053123_765.webp)
WB analysis of various samples using GTX03239 PER3 antibody [GT1327]. Dilution : 1:1000 Loading : 25microg per lane
PER3 antibody [GT1327]
GTX03239
ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
Product group Antibodies
TargetPER3
Overview
- SupplierGeneTex
- Product NamePER3 antibody [GT1327] - Orthogonal Validated
- Delivery Days Customer9
- Application Supplier NoteWB: 1:500 - 1:2000. ICC/IF: 1:50 - 1:200. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
- ApplicationsImmunoFluorescence, Western Blot, ImmunoCytoChemistry
- CertificationResearch Use Only
- ClonalityMonoclonal
- Clone IDGT1327
- Concentration2.44 mg/ml
- ConjugateUnconjugated
- Gene ID8863
- Target namePER3
- Target descriptionperiod circadian regulator 3
- Target synonymsFASPS3, GIG13, period circadian protein homolog 3, cell growth-inhibiting gene 13 protein, circadian clock protein PERIOD 3, period circadian clock 3, period circadian protein 3
- HostRabbit
- IsotypeIgG
- Protein IDP56645
- Protein NamePeriod circadian protein homolog 3
- Scientific DescriptionThis gene is a member of the Period family of genes and is expressed in a circadian pattern in the suprachiasmatic nucleus, the primary circadian pacemaker in the mammalian brain. Genes in this family encode components of the circadian rhythms of locomotor activity, metabolism, and behavior. This gene is upregulated by CLOCK/ARNTL heterodimers but then represses this upregulation in a feedback loop using PER/CRY heterodimers to interact with CLOCK/ARNTL. Polymorphisms in this gene have been linked to sleep disorders. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2014]
- Storage Instruction-20°C or -80°C,2°C to 8°C
- UNSPSC12352203
![ICC/IF analysis of NIH-3T3 cells using GTX03239 PER3 antibody [GT1327]. Blue : DAPI for nuclear staining Dilution : 1:100 ICC/IF analysis of NIH-3T3 cells using GTX03239 PER3 antibody [GT1327]. Blue : DAPI for nuclear staining Dilution : 1:100](https://www.genetex.com/upload/website/prouct_img/normal/GTX03239/GTX03239_20210615_ICCIF_13_w_23053123_300.webp)
![Various whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced. Various whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://www.genetex.com/upload/website/prouct_img/normal/GTX03239/GTX03239_4000001893_20210716_WB_2_w_23053123_260.webp)
![Various whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody. Various whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.](https://www.genetex.com/upload/website/prouct_img/normal/GTX03239/GTX03239_4000001893_20210716_WB_3_w_23053123_951.webp)
![Untreated (-) and treated (+) 293T whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced. Untreated (-) and treated (+) 293T whole cell extracts (30 microg) were separated by 5% SDS-PAGE, and the membrane was blotted with PER3 antibody [GT1327] (GTX03239) diluted at 1:500. The HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody, and the signal was developed with Trident ECL plus-Enhanced.](https://www.genetex.com/upload/website/prouct_img/normal/GTX03239/GTX03239_4000001893_20210716_WB_treatment_Serum_w_23053123_161.webp)







