e faecalis atcc 14506 Search Results


atcc 14506  (ATCC)
95
ATCC atcc 14506
Atcc 14506, supplied by ATCC, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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zone mic e feacalis atcc 14506 10 00  (ATCC)
92
ATCC zone mic e feacalis atcc 14506 10 00
Zone Mic E Feacalis Atcc 14506 10 00, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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staphylococcus aureus atcc 25923 enterococcus faecalis atcc 14506 gram  (ATCC)
99
ATCC staphylococcus aureus atcc 25923 enterococcus faecalis atcc 14506 gram
Staphylococcus Aureus Atcc 25923 Enterococcus Faecalis Atcc 14506 Gram, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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14506 a hydrophilia atcc 7966 e coli atcc 10536 e aerogenes atcc 13048 p mirabilis atcc 12453 p vulgaris atcc 33420 s typhimurium atcc 51812 s sonnei atcc 29930 s marcescens atcc 13880 v parahaemolyticus atcc 17802 p aeruginosa atcc 10145 c albicans atcc 90028 c parapsilosis atcc 22019  (ATCC)
99
ATCC 14506 a hydrophilia atcc 7966 e coli atcc 10536 e aerogenes atcc 13048 p mirabilis atcc 12453 p vulgaris atcc 33420 s typhimurium atcc 51812 s sonnei atcc 29930 s marcescens atcc 13880 v parahaemolyticus atcc 17802 p aeruginosa atcc 10145 c albicans atcc 90028 c parapsilosis atcc 22019
14506 A Hydrophilia Atcc 7966 E Coli Atcc 10536 E Aerogenes Atcc 13048 P Mirabilis Atcc 12453 P Vulgaris Atcc 33420 S Typhimurium Atcc 51812 S Sonnei Atcc 29930 S Marcescens Atcc 13880 V Parahaemolyticus Atcc 17802 P Aeruginosa Atcc 10145 C Albicans Atcc 90028 C Parapsilosis Atcc 22019, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/14506 a hydrophilia atcc 7966 e coli atcc 10536 e aerogenes atcc 13048 p mirabilis atcc 12453 p vulgaris atcc 33420 s typhimurium atcc 51812 s sonnei atcc 29930 s marcescens atcc 13880 v parahaemolyticus atcc 17802 p aeruginosa atcc 10145 c albicans atcc 90028 c parapsilosis atcc 22019/product/ATCC
Average 99 stars, based on 1 article reviews
14506 a hydrophilia atcc 7966 e coli atcc 10536 e aerogenes atcc 13048 p mirabilis atcc 12453 p vulgaris atcc 33420 s typhimurium atcc 51812 s sonnei atcc 29930 s marcescens atcc 13880 v parahaemolyticus atcc 17802 p aeruginosa atcc 10145 c albicans atcc 90028 c parapsilosis atcc 22019 - by Bioz Stars, 2026-03
99/100 stars
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brucella  (ATCC)
99
ATCC brucella
Brucella, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 99 stars, based on 1 article reviews
brucella - by Bioz Stars, 2026-03
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pathogen indicators  (ATCC)
99
ATCC pathogen indicators
Pathogen Indicators, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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pathogen indicators - by Bioz Stars, 2026-03
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nr1d1  (Proteintech)
94
Proteintech nr1d1
LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, <t>NR1D1</t> and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.
Nr1d1, 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
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slc6a1 rabbit  (ABclonal Biotechnology)
90
ABclonal Biotechnology slc6a1 rabbit
LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, <t>NR1D1</t> and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.
Slc6a1 Rabbit, 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
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bis(hexamethylene)triamine (#14506)  (Millipore)
90
Millipore bis(hexamethylene)triamine (#14506)
LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, <t>NR1D1</t> and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.
Bis(Hexamethylene)Triamine (#14506), supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti-human igg-hrp  (Millipore)
90
Millipore anti-human igg-hrp
LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, <t>NR1D1</t> and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.
Anti Human Igg Hrp, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fischer 1982  (DSMZ)
86
DSMZ fischer 1982
LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, <t>NR1D1</t> and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.
Fischer 1982, supplied by DSMZ, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, NR1D1 and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.

Journal: Molecular Metabolism

Article Title: Long non-coding RNA LncCplx2 regulates glucose homeostasis and pancreatic β cell function

doi: 10.1016/j.molmet.2024.101878

Figure Lengend Snippet: LncCplx2 expression is regulated by BMAL1. (A) ChIP-qPCR assays demonstrating enrichment of BMAL1 at the LncCplx2 promoter region in Min6 cells. RNA Polymerase II antibody and IgG serve as the positive and negative control, respectively (n = 3/2). Two different primer pairs ( LncCplx2 -P1 and LncCplx2 -P2) targeted the promoter of LncCplx2 were used for the PCR assay. IB analysis of BMAL1, NR1D1 and E4BP4 antibody immunoprecipitation efficiency, IgG as negative control. (B) IB analysis of BMAL1 protein level in Bmal1 KO and control Min6 cells. β-Actin was used as the loading control. (C) LncCplx2 expression was analyzed by qRT-PCR in Bmal1 KO and control Min6 cells (n = 4). (D) qRT-PCR analysis of Bmal1 and LncCplx2 expression in Min6 cells expressing two shRNAs targeting Bmal1 and scrambled shRNA as control (n = 3). (E) Effects of Bmal1 overexpression on different luciferase reporter activity driven by the LncCplx2 promoter and negative control (n = 6). All the data are shown as the mean ± SEM. ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001, using two-tailed Student's t-test and one-way ANOVA.

Article Snippet: The membranes were incubated with primary antibodies against Tubulin (Proteintech, 66031-1-Ig), DDX1 (Proteintech, 11357-1-AP), SETD8 (Abcam, ab111691), HistoneH3 (Invitrogen, PA5-16183), CPLX2 (Proteintech, 18149-1-AP), BMAL1 (Invitrogen, PA1-46118), E4BP4 (Proteintech, 11773-1-AP), NR1D1 (Proteintech, 14506-1-AP), EZH2 (Invitrogen, 36-6300), and β-actin (Sigma Aldrich, A1978), followed by the appropriate HRP-conjugated secondary antibodies (Proteintech, SA00001-2/SA00001-1), and protein expression was detected with enhanced luminescence reagents (GE Healthcare, RPN2106).

Techniques: Expressing, ChIP-qPCR, Negative Control, Immunoprecipitation, Control, Quantitative RT-PCR, shRNA, Over Expression, Luciferase, Activity Assay, Two Tailed Test