clock anti rabbit Search Results


clock antibody  (Bio-Techne corporation)
94
Bio-Techne corporation clock antibody
Clock Antibody, supplied by Bio-Techne corporation, 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/result/clock antibody/product/Bio-Techne corporation
Average 94 stars, based on 1 article reviews
clock antibody - by Bioz Stars, 2026-06
94/100 stars
  Buy from Supplier
rabbit anti-clock  (ABclonal Biotechnology)
90
ABclonal Biotechnology rabbit anti-clock
Rabbit Anti Clock, supplied by ABclonal Biotechnology, 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/result/rabbit anti-clock/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
rabbit anti-clock - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
biotin-labeled goat anti-rabbit secondary antibody for clock  (Beijing CWBio)
90
Beijing CWBio biotin-labeled goat anti-rabbit secondary antibody for clock
Immunohistochemistry staining of <t>CLOCK</t> <t>and</t> <t>PER2</t> in paraffin sections of human ovaries. Staining of CLOCK was detected in the cumulus cells and mural granulosa cells, absent in the theca cells of the dominant antral follicles (D2, E2), and present in the interstitial cells, but absent in primordial follicles (A2), primary follicles (B2), and preantral follicles (C2). Staining of PER2 was present in the cumulus cells, mural granulosa cells, weak in the theca cells of dominant antral follicles (D3, E3), and present in the interstitial cells, but absent in the primordial follicles (A3), primary follicles (B3), and preantral follicles (C3). A1 to E1 are negative controls (no primary antibody) of the primordial, primary, preantral, and antral follicles and the cumulus complex, respectively. Bars = 50 μm. Original magnification, ×200
Biotin Labeled Goat Anti Rabbit Secondary Antibody For Clock, supplied by Beijing CWBio, 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/result/biotin-labeled goat anti-rabbit secondary antibody for clock/product/Beijing CWBio
Average 90 stars, based on 1 article reviews
biotin-labeled goat anti-rabbit secondary antibody for clock - by Bioz Stars, 2026-06
90/100 stars
  Buy from Supplier
rabbit anti-human clock polyclonal antibody  (Cusabio)
N/A
Rabbit anti-Human CLOCK Polyclonal Antibody
   Buy from Supplier
rabbit anti human clock polyclonal affinity purified  (Innovative Research Inc)
N/A
Rabbit Anti Human CLOCK Polyclonal Affinity Purified (PBS with 0.02% sodium azide, 50% glycerol, pH7.3) (Western Blot) from Innovative Research is a polyclonal antibody in a liquid format, buffered in PBS with 0.02% sodium azide,
   Buy from Supplier
rabbit anti human clock monoclonal clone acch-3  (Innovative Research Inc)
N/A
Rabbit Anti Human CLOCK Monoclonal Clone ACCH-3 from Innovative Research is a monoclonal antibody in a Liquid format, buffered in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol, 0.4-0.5mg/ml BSA.
   Buy from Supplier
rabbit anti-human clock (center)  (RayBiotech)
N/A
Rabbit Anti-Human CLOCK (Center) Antibody, 400 µl
   Buy from Supplier
rabbit anti-clock antibody  (RayBiotech)
N/A
Rabbit Anti-CLOCK Antibody, (100 µg)
   Buy from Supplier
rabbit anti- clock polyclonal antibody  (Cusabio)
N/A
Rabbit anti-Human CLOCK Polyclonal Antibody
   Buy from Supplier

Image Search Results


Immunohistochemistry staining of CLOCK and PER2 in paraffin sections of human ovaries. Staining of CLOCK was detected in the cumulus cells and mural granulosa cells, absent in the theca cells of the dominant antral follicles (D2, E2), and present in the interstitial cells, but absent in primordial follicles (A2), primary follicles (B2), and preantral follicles (C2). Staining of PER2 was present in the cumulus cells, mural granulosa cells, weak in the theca cells of dominant antral follicles (D3, E3), and present in the interstitial cells, but absent in the primordial follicles (A3), primary follicles (B3), and preantral follicles (C3). A1 to E1 are negative controls (no primary antibody) of the primordial, primary, preantral, and antral follicles and the cumulus complex, respectively. Bars = 50 μm. Original magnification, ×200

Journal: Journal of Ovarian Research

Article Title: Expression pattern of circadian genes and steroidogenesis-related genes after testosterone stimulation in the human ovary

doi: 10.1186/s13048-016-0264-5

Figure Lengend Snippet: Immunohistochemistry staining of CLOCK and PER2 in paraffin sections of human ovaries. Staining of CLOCK was detected in the cumulus cells and mural granulosa cells, absent in the theca cells of the dominant antral follicles (D2, E2), and present in the interstitial cells, but absent in primordial follicles (A2), primary follicles (B2), and preantral follicles (C2). Staining of PER2 was present in the cumulus cells, mural granulosa cells, weak in the theca cells of dominant antral follicles (D3, E3), and present in the interstitial cells, but absent in the primordial follicles (A3), primary follicles (B3), and preantral follicles (C3). A1 to E1 are negative controls (no primary antibody) of the primordial, primary, preantral, and antral follicles and the cumulus complex, respectively. Bars = 50 μm. Original magnification, ×200

Article Snippet: Slides were washed and incubated with biotin-labeled goat anti-rabbit secondary antibody for CLOCK (CWBIO) or bovine anti-goat secondary antibody for PER2 (Santa Cruz Biotechnology) for 30 min, then washed and incubated with horseradish peroxidase-labeled streptavidin for 10 min.

Techniques: Immunohistochemistry, Staining

Expression patterns of circadian genes after testosterone treatment in human luteinized granulosa cells. Human luteinized granulosa cells were exposed to 100 ng/mL testosterone dissolved in serum-free medium for 2 h and cells in the control group were cultured in serum-free medium without treatment. Samples were harvested every 4 h from the beginning of treatment for 48 h. Each value represents the mean ± SEM of three independent experiments. Significant statistical differences are shown as below: the testosterone group PER2 P 4 vs. 24 = 0.028, P 24 vs. 32 = 0.041, P 24 vs. 48 = 0.039, P 4 vs. 44 = 0.024, CLOCK P 4 vs. 24 = 0.04; the control group PER2 P 4 vs. 16 = 0.016, CLOCK P 4 vs. 12 = 0.022, P 4 vs. 16 = 0.031, P 4 vs. 20 = 0.006, P 4 vs. 36 = 0.011

Journal: Journal of Ovarian Research

Article Title: Expression pattern of circadian genes and steroidogenesis-related genes after testosterone stimulation in the human ovary

doi: 10.1186/s13048-016-0264-5

Figure Lengend Snippet: Expression patterns of circadian genes after testosterone treatment in human luteinized granulosa cells. Human luteinized granulosa cells were exposed to 100 ng/mL testosterone dissolved in serum-free medium for 2 h and cells in the control group were cultured in serum-free medium without treatment. Samples were harvested every 4 h from the beginning of treatment for 48 h. Each value represents the mean ± SEM of three independent experiments. Significant statistical differences are shown as below: the testosterone group PER2 P 4 vs. 24 = 0.028, P 24 vs. 32 = 0.041, P 24 vs. 48 = 0.039, P 4 vs. 44 = 0.024, CLOCK P 4 vs. 24 = 0.04; the control group PER2 P 4 vs. 16 = 0.016, CLOCK P 4 vs. 12 = 0.022, P 4 vs. 16 = 0.031, P 4 vs. 20 = 0.006, P 4 vs. 36 = 0.011

Article Snippet: Slides were washed and incubated with biotin-labeled goat anti-rabbit secondary antibody for CLOCK (CWBIO) or bovine anti-goat secondary antibody for PER2 (Santa Cruz Biotechnology) for 30 min, then washed and incubated with horseradish peroxidase-labeled streptavidin for 10 min.

Techniques: Expressing, Cell Culture