per1 Search Results


per1 rabbit nbp2 24589  (Novus Biologicals)
94
Novus Biologicals per1 rabbit nbp2 24589
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Per1 Rabbit Nbp2 24589, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pmc11213646-94-19-22?v=Novus+Biologicals
Average 94 stars, based on 1 article reviews
per1 rabbit nbp2 24589 - by Bioz Stars, 2026-08
94/100 stars
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antibody rrid  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology antibody rrid
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Antibody Rrid, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pm34943821-95-38-48?v=Santa+Cruz+Biotechnology
Average 93 stars, based on 1 article reviews
antibody rrid - by Bioz Stars, 2026-08
93/100 stars
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per1 biorbyt orb374136  (Biorbyt)
91
Biorbyt per1 biorbyt orb374136
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Per1 Biorbyt Orb374136, supplied by Biorbyt, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pmc09925306__thnov13p1130s1-51-59-60?v=Biorbyt
Average 91 stars, based on 1 article reviews
per1 biorbyt orb374136 - by Bioz Stars, 2026-08
91/100 stars
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per1 male mice  (Cyagen Biosciences)
91
Cyagen Biosciences per1 male mice
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Per1 Male Mice, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/10__1523_slash_jneurosci__1914___22__2023-58-0-10?v=Cyagen+Biosciences
Average 91 stars, based on 1 article reviews
per1 male mice - by Bioz Stars, 2026-08
91/100 stars
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13463 1 ap anti per2 proteintech  (Proteintech)
94
Proteintech 13463 1 ap anti per2 proteintech
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
13463 1 Ap Anti Per2 Proteintech, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pmc10478628__mjad012_supplemental_file-24-91-93?v=Proteintech
Average 94 stars, based on 1 article reviews
13463 1 ap anti per2 proteintech - by Bioz Stars, 2026-08
94/100 stars
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pcmv6 per1  (OriGene)
90
OriGene pcmv6 per1
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Pcmv6 Per1, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pmc04874896-120-36-42?v=OriGene
Average 90 stars, based on 1 article reviews
pcmv6 per1 - by Bioz Stars, 2026-08
90/100 stars
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plasmid dna  (OriGene)
90
OriGene plasmid dna
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Plasmid Dna, supplied by OriGene, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pm34237069-340-3-11?v=OriGene
Average 90 stars, based on 1 article reviews
plasmid dna - by Bioz Stars, 2026-08
90/100 stars
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syn flex mruby2 gsg p2a gcamp6s wpre sv40  (Addgene inc)
90
Addgene inc syn flex mruby2 gsg p2a gcamp6s wpre sv40
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Syn Flex Mruby2 Gsg P2a Gcamp6s Wpre Sv40, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/10__1523_slash_jneurosci__1732___20__2021-61-0-26?v=Addgene+inc
Average 90 stars, based on 1 article reviews
syn flex mruby2 gsg p2a gcamp6s wpre sv40 - by Bioz Stars, 2026-08
90/100 stars
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rabbit monoclonal anti per1  (Novus Biologicals)
91
Novus Biologicals rabbit monoclonal anti per1
Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) <t>PER1</t> protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.
Rabbit Monoclonal Anti Per1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pm37434152-239-59-92?v=Novus+Biologicals
Average 91 stars, based on 1 article reviews
rabbit monoclonal anti per1 - by Bioz Stars, 2026-08
91/100 stars
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anti per1 antibody  (OriGene)
93
OriGene anti per1 antibody
Representative pictures of positive and negative expression of <t>PER1</t> protein in BC tissues (100× and 400×). ( A ) Positive expression. ( B ) Negative expression.
Anti Per1 Antibody, supplied by OriGene, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/pmc12348893-121-8-10?v=OriGene
Average 93 stars, based on 1 article reviews
anti per1 antibody - by Bioz Stars, 2026-08
93/100 stars
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per1  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology per1
Representative pictures of positive and negative expression of <t>PER1</t> protein in BC tissues (100× and 400×). ( A ) Positive expression. ( B ) Negative expression.
Per1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/per1/10__3390_slash_molecules23040745-153-7-14?v=Santa+Cruz+Biotechnology
Average 93 stars, based on 1 article reviews
per1 - by Bioz Stars, 2026-08
93/100 stars
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Image Search Results


Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) PER1 protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.

Journal: Physiological Reports

Article Title: BMAL1 sex‐specific effects in the neonatal mouse airway exposed to moderate hyperoxia

doi: 10.14814/phy2.16122

Figure Lengend Snippet: Bmal1 WT, Het, and KO protein expression validation. (a) BMAL1 protein expression from Bmal1 WT, Het, and KO male and female neonatal whole lung mouse tissue measured by Jess automated and quantitative immuno‐capillary assay that generates a digital Western blot (representative image shown). ~0.3 mg protein loaded per capillary. BMAL1 peaks were identified using a molecular weight of ~86 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–9 pups per group. (b) PER1 protein expression using ~0.6 mg protein loaded per capillary based on antibody optimization in Jess. PER1 peaks were identified at a molecular weight of ~50 kDa. Protein expression was normalized using chemiluminescence of total protein (values indicated on representative image). Ordinary two‐way ANOVA was used to compare Bmal1 genotype and O 2 exposure groups in each sex. Data are represented as mean ± SD; n = 3–4 pups per group.

Article Snippet: The following primary antibodies were used: BMAL1 (D2L7G) Rabbit mAb #14020 (Cell Signaling Technology; Danvers, MA, USA) at 1:25; PER1 Rabbit NBP2‐24589 (Novus Biologicals; Centennial, CO, USA) at 1:50; Fibronectin Rabbit ab2413 (Abcam; Cambridge, UK) at 1:200; Collagen I Rabbit ab34710 (Abcam; Cambridge, UK) at 1:20; Collagen III Rabbit ab7778 (Abcam; Cambridge, UK) at 1:20.

Techniques: Expressing, Biomarker Discovery, Western Blot, Molecular Weight

Representative pictures of positive and negative expression of PER1 protein in BC tissues (100× and 400×). ( A ) Positive expression. ( B ) Negative expression.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: Representative pictures of positive and negative expression of PER1 protein in BC tissues (100× and 400×). ( A ) Positive expression. ( B ) Negative expression.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques: Expressing

PER1 affects BC patient’s prognosis. ( A ) RFS and OS of 172 BC patients based on the ten-year follow‑up data. ( B ) RFS and OS in lymph node metastasis subgroup. ( C ) RFS and OS in vascular tumor thrombus subgroup.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: PER1 affects BC patient’s prognosis. ( A ) RFS and OS of 172 BC patients based on the ten-year follow‑up data. ( B ) RFS and OS in lymph node metastasis subgroup. ( C ) RFS and OS in vascular tumor thrombus subgroup.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques:

The key protein expression of the MAPK pathway in the breast cancer cell with low and high PER1 expression. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs Lenti-blast-KB group.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: The key protein expression of the MAPK pathway in the breast cancer cell with low and high PER1 expression. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs Lenti-blast-KB group.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques: Expressing

Effects of ERK5 inhibitor XMD17-109 on MEK5/ERK5 pathway activity. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: Effects of ERK5 inhibitor XMD17-109 on MEK5/ERK5 pathway activity. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques: Activity Assay

XMD17-109 reverses the enhancement of the proliferative ability in BC cells with low expression of PER1 (100×). ( A ) Colony Formation Assay. ( B ) EdU Assay. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: XMD17-109 reverses the enhancement of the proliferative ability in BC cells with low expression of PER1 (100×). ( A ) Colony Formation Assay. ( B ) EdU Assay. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques: Expressing, Colony Assay, EdU Assay

XMD17-109 reverses the increased migration and invasion ability in BC cells with low expression of PER1 (100×). ( A ) Transwell tumor cell migration assay. ( B ) Transwell tumor cell invasion assay. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Journal: International Journal of General Medicine

Article Title: PER1 Serves as a Tumor Suppressor in Breast Cancer by Regulating MEK5/ERK5 Signaling Pathway

doi: 10.2147/IJGM.S511530

Figure Lengend Snippet: XMD17-109 reverses the increased migration and invasion ability in BC cells with low expression of PER1 (100×). ( A ) Transwell tumor cell migration assay. ( B ) Transwell tumor cell invasion assay. * P <0.05 vs pGenesil-1-KB group; # P <0.05 vs pGenesil-1-PER1 group.

Article Snippet: The sections were then incubated overnight in primary anti-PER1 antibody (OriGene Technologies, Inc.) at 1:100 dilution at 4 °C, warmed for 1 h at AT, rinsed three times with PBS, and incubated in undiluted secondary antibody goat anti-rabbit IgG-HRP (OriGene Technologies, Inc.) at AT for 1 h. For the negative control, the primary antibody was replaced with PBS.

Techniques: Migration, Expressing, Cell Migration Assay, Invasion Assay