Antibody data
- Antibody Data
- Antigen structure
- References [1]
- Comments [0]
- Validations
- Western blot [1]
- Other assay [2]
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- Product number
- PA5-38634 - Provider product page
- Provider
- Invitrogen Antibodies
- Product name
- Anti-PER3 Polyclonal Antibody
- Antibody type
- Polyclonal
- Antigen
- Synthetic peptide
- Reactivity
- Human
- Host
- Rabbit
- Isotype
- IgG
- Vial size
- 100 µg
- Concentration
- 1 mg/mL
- Storage
- -20°C
Submitted references Core circadian clock gene expression in human dental pulp-derived cells in response to L-mimosine, hypoxia and echinomycin.
Janjić K, Kurzmann C, Moritz A, Agis H
European journal of oral sciences 2018 Aug;126(4):263-271
European journal of oral sciences 2018 Aug;126(4):263-271
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Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Western blot analysis of PER3/Period Circadian Protein 3 in extracts from Jurkat cells treated with insulin (0.01U/mL, 15 min) using a PER3/Period Circadian Protein 3 polyclonal antibody (Product # PA5-38634).
Supportive validation
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 3 Effect of L-mimosine (L- MIM ), hypoxia and echinomycin on the levels of core clock proteins in two-dimensional (2D) monolayer and three-dimensional (3D) spheroid cultures of dental pulp-derived cells ( DPC ). The DPC in 2D monolayer cultures were treated with L- MIM or hypoxia (A) and with L- MIM or hypoxia in combination with echinomycin or with echinomycin alone (C) for 24 h. Further DPC were cultured in 3D spheroid cultures and treated with L- MIM or hypoxia (B). The amounts of circadian locomotor output cycles kaput ( CLOCK ), cryptochrome circadian regulator 1 and 2 ( CRY 1 and CRY 2, respectively) and period circadian regulator 3 ( PER 3) proteins produced were detected by western blotting. Glyceraldehyde-3-phosphate dehydrogenase ( GAPDH ) was used as reference protein. Experiments were conducted at least twice with DPC from two different donors ( n = 4).
- Submitted by
- Invitrogen Antibodies (provider)
- Main image
- Experimental details
- Figure 4 Core clock gene mRNA and protein levels under normoxia, L-mimosine (L- MIM ) and hypoxia change during the observation period. Dental pulp-derived cells ( DPC ) in two-dimensional (2D) monolayer cultures were serum-starved and afterwards treated with L- MIM or hypoxia. mRNA (A-D) and protein (E-I) levels of circadian locomotor output cycles kaput ( CLOCK ), cryptochrome circadian regulator 1 and 2 ( CRY 1 and CRY 2, respectively) and period circadian regulator 3 ( PER 3) were measured in a 4-h interval over 48 h by quantitative PCR ( qPCR ) and western blotting, respectively. mRNA levels are displayed relative to glyceraldehyde-3-phosphate dehydrogenase ( GAPDH ) and 0 h after serum starvation (A-D). GAPDH was used as reference protein (E-I). Experiments were conducted at least twice with DPC from two different donors ( n = 4).