psychophysics toolbox extension (ptb-3) Search Results


96
MathWorks Inc psychophysics toolbox extension
Psychophysics Toolbox Extension, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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MathWorks Inc source toolbox psychophysics toolbox version 3 ptb 3
Source Toolbox Psychophysics Toolbox Version 3 Ptb 3, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/psychophysics+toolbox+extension+(ptb-3)/Instrument+Control+Toolbox/10__1177_slash_2331216518816600-77-7-16
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source toolbox psychophysics toolbox version 3 ptb 3 - by Bioz Stars, 2026-09
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MathWorks Inc psychophysics toolbox version 3 ptb 3
Psychophysics Toolbox Version 3 Ptb 3, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/psychophysics+toolbox+extension+(ptb-3)/Audio+Toolbox/pmc04124486-77-12-20
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psychophysics toolbox version 3 ptb 3 - by Bioz Stars, 2026-09
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MathWorks Inc psychophysics toolbox
Psychophysics Toolbox, supplied by MathWorks Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/psychophysics+toolbox+extension+(ptb-3)/Control+System+Toolbox/pm40097556-92-4-9
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psychophysics toolbox - by Bioz Stars, 2026-09
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93
Proteintech ptbp1 protein
Figure 8. NDRG1 and <t>PTBP1</t> collaborate to promote EndMT. (A) The Nuclear and cytoplasm proteins of input, IgG and anti-His-Tag were purified and size fractionated on 10% SDS-PAGE. The gel was stained by coomassie brilliant blue staining. (B) The content of NDRG1 was analyzed by NDRG1 antibody. (C) The Co-IP experiment detecting the interaction between NDRG1 and PTBP1 in nucleus from HUVEC treated with H2O2 (200 μM) and TGF-β (50 ng/mL, 48 h). (D, E) Molecular simulations and protein docking of NDRG1 and PTBP1. (F) Schematic diagrams of 6*His-Tagged full-length (WT) NDRG1, and their various deletion mutants (180-294aa, and 326-394aa) (Top). HEK 293T cells were co-transfected with His-Tagged NDRG1 or its deletion mutants or vectors, and whole cell lysates were assessed by immunoprecipitation followed by immunoblotting with
Ptbp1 Protein, supplied by Proteintech, 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/psychophysics+toolbox+extension+(ptb-3)/PTBP1+Fusion+Protein/pm39744686-139-4-7
Average 93 stars, based on 1 article reviews
ptbp1 protein - by Bioz Stars, 2026-09
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90
OriGene entrez nucleotide
KEY RESOURCES TABLE
Entrez Nucleotide, 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/psychophysics+toolbox+extension+(ptb-3)/Ptbp1+(NM_008956)+Mouse+Tagged+ORF+Clone/pmc07580783-854-253-251
Average 90 stars, based on 1 article reviews
entrez nucleotide - by Bioz Stars, 2026-09
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90
OriGene full length ptbp1 expression vector
(A) RNA ploy II ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). (B) Left: western blot analysis of <t>PTBP1</t> in hLMR1 pulldown, right: expression of hLMR1 in PTBP1 RIP (RNA immunoprecipitation) in humanized liver. (C) HMGCS1 promoter-driven luciferase reporter assay in 293A cells (n=3 for each group). Data are representative results of three independent experiments. (D) PTBP1 ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). Error bars represent SEM, * p<0.05.
Full Length Ptbp1 Expression Vector, 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/psychophysics+toolbox+extension+(ptb-3)/PTBP1+(NM_002819)+Human+Tagged+ORF+Clone/bio_rxiv__2020__01__01__884023-260-0-10
Average 90 stars, based on 1 article reviews
full length ptbp1 expression vector - by Bioz Stars, 2026-09
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93
OriGene ptbp1 1
(A) RNA ploy II ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). (B) Left: western blot analysis of <t>PTBP1</t> in hLMR1 pulldown, right: expression of hLMR1 in PTBP1 RIP (RNA immunoprecipitation) in humanized liver. (C) HMGCS1 promoter-driven luciferase reporter assay in 293A cells (n=3 for each group). Data are representative results of three independent experiments. (D) PTBP1 ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). Error bars represent SEM, * p<0.05.
Ptbp1 1, 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/psychophysics+toolbox+extension+(ptb-3)/PTBP1+(NM_031991)+Human+Tagged+ORF+Clone+Lentiviral+Particle/pmc12618068__jci-135-182100-s292-94-18-34
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ptbp1 1 - by Bioz Stars, 2026-09
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94
Proteintech tsa system
(A) RNA ploy II ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). (B) Left: western blot analysis of <t>PTBP1</t> in hLMR1 pulldown, right: expression of hLMR1 in PTBP1 RIP (RNA immunoprecipitation) in humanized liver. (C) HMGCS1 promoter-driven luciferase reporter assay in 293A cells (n=3 for each group). Data are representative results of three independent experiments. (D) PTBP1 ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). Error bars represent SEM, * p<0.05.
Tsa System, 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/psychophysics+toolbox+extension+(ptb-3)/PTBP1+Antibody/pmc06971890__12943_2019_1122_MOESM1_ESM-40-8-26
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92
Proteintech western blot analysis
gRNA-dependent off-target binding alters the expression of essential genes and induces substantial alterations in cell proliferation. ( A – D ) RT-qPCR and <t>western</t> <t>blot</t> analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the PspCas13b-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. ( E – H ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the RfxCas13d-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. RT-qPCR data are presented as mean ± SD ( n = 3). Relative changes in protein abundance were quantified by densitometric <t>analysis</t> and are indicated as red numbers at the bottom of each panel. ( I ) Proliferation of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or a non-targeting control gRNA (gNT), measured by CCK-8 assay. Proliferation rates were measured by absorbance at days 1–5 and normalized to that at day 1. Data are presented as mean ± SD ( n = 4). * P < 0.05; ** P < 0.01; *** P < 0.001. ns, not significant. ( J ) Apoptosis analysis of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or non-targeting control gRNA (gNT). Data are presented as mean ± SD ( n = 3). ns, not significant.
Western Blot Analysis, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/psychophysics+toolbox+extension+(ptb-3)/PTBP1+Polyclonal+antibody/pmc12926919-68-6-15
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90
OriGene full length ptbp1
gRNA-dependent off-target binding alters the expression of essential genes and induces substantial alterations in cell proliferation. ( A – D ) RT-qPCR and <t>western</t> <t>blot</t> analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the PspCas13b-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. ( E – H ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the RfxCas13d-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. RT-qPCR data are presented as mean ± SD ( n = 3). Relative changes in protein abundance were quantified by densitometric <t>analysis</t> and are indicated as red numbers at the bottom of each panel. ( I ) Proliferation of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or a non-targeting control gRNA (gNT), measured by CCK-8 assay. Proliferation rates were measured by absorbance at days 1–5 and normalized to that at day 1. Data are presented as mean ± SD ( n = 4). * P < 0.05; ** P < 0.01; *** P < 0.001. ns, not significant. ( J ) Apoptosis analysis of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or non-targeting control gRNA (gNT). Data are presented as mean ± SD ( n = 3). ns, not significant.
Full Length Ptbp1, 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/psychophysics+toolbox+extension+(ptb-3)/PTBP1+(NM_002819)+Human+Untagged+Clone/pm31358321-45-0-19
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Image Search Results


Figure 8. NDRG1 and PTBP1 collaborate to promote EndMT. (A) The Nuclear and cytoplasm proteins of input, IgG and anti-His-Tag were purified and size fractionated on 10% SDS-PAGE. The gel was stained by coomassie brilliant blue staining. (B) The content of NDRG1 was analyzed by NDRG1 antibody. (C) The Co-IP experiment detecting the interaction between NDRG1 and PTBP1 in nucleus from HUVEC treated with H2O2 (200 μM) and TGF-β (50 ng/mL, 48 h). (D, E) Molecular simulations and protein docking of NDRG1 and PTBP1. (F) Schematic diagrams of 6*His-Tagged full-length (WT) NDRG1, and their various deletion mutants (180-294aa, and 326-394aa) (Top). HEK 293T cells were co-transfected with His-Tagged NDRG1 or its deletion mutants or vectors, and whole cell lysates were assessed by immunoprecipitation followed by immunoblotting with

Journal: Theranostics

Article Title: PIM1 instigates endothelial-to-mesenchymal transition to aggravate atherosclerosis.

doi: 10.7150/thno.102597

Figure Lengend Snippet: Figure 8. NDRG1 and PTBP1 collaborate to promote EndMT. (A) The Nuclear and cytoplasm proteins of input, IgG and anti-His-Tag were purified and size fractionated on 10% SDS-PAGE. The gel was stained by coomassie brilliant blue staining. (B) The content of NDRG1 was analyzed by NDRG1 antibody. (C) The Co-IP experiment detecting the interaction between NDRG1 and PTBP1 in nucleus from HUVEC treated with H2O2 (200 μM) and TGF-β (50 ng/mL, 48 h). (D, E) Molecular simulations and protein docking of NDRG1 and PTBP1. (F) Schematic diagrams of 6*His-Tagged full-length (WT) NDRG1, and their various deletion mutants (180-294aa, and 326-394aa) (Top). HEK 293T cells were co-transfected with His-Tagged NDRG1 or its deletion mutants or vectors, and whole cell lysates were assessed by immunoprecipitation followed by immunoblotting with

Article Snippet: PIM1 protein (HY-P701745, MCE), PTBP1 protein (Ag28404, Proteintech), and small molecule Max-40279 (HY-145723, MCE; 500 nM) binding activities were generated with the SPR system, and the binding signal was exhibited by the response (RU) value.

Techniques: Purification, SDS Page, Staining, Co-Immunoprecipitation Assay, Transfection, Immunoprecipitation, Western Blot

KEY RESOURCES TABLE

Journal: Neuron

Article Title: Selective neuronal vulnerability in Alzheimer’s disease: a network-based analysis

doi: 10.1016/j.neuron.2020.06.010

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Psy., 2018 RRID: NA Mouse: htau PAC: B6.Cg- Mapt tm1(EGFP)Klt Tg(MAPT)8cPdav/J Jackson lab IMSR Cat# JAX:005491, RRID:IMSR_JAX:005491 Oligonucleotides all mouse genotyping primers See Table S7 for sequences IDT-DNA, RRID : NA fluorescent PCR for human tau splicing - forward primer IDT-DNA HPLC purified 5’-IRDye 800 – CTCCAAAATCAGGGGATCGC – 3’, RRID: NA fluorescent PCR for human tau splicing - reverse primer IDT-DNA unlabeled 5’ –CCTTGCTCAGGTCAACTGGT – 3’, RRID: NA fluorescent PCR for mouse tau splicing - forward primer IDT-DNA HPLC purified 5’-IRDye 800 – CACCAAAATCCGGAGAACGA – 3’, RRID: NA fluorescent PCR for mouse tau splicing - reverse primer IDT-DNA unlabeled 5’ –CTTTGCTCAGGTCCACCGG – 3’, RRID: NA Recombinant DNA RP23–329L1 unmodified BAC CHORI RRID : NA RP23–181A2 unmodified BAC CHORI RRID : NA RP24–68J22 unmodified BAC CHORI RRID : NA RP23–307B16 unmodified BAC CHORI RRID : NA RP23–199D5 unmodified BAC CHORI RRID : NA RP24–344N1 unmodified BAC CHORI RRID : NA RP23–126C5 unmodified BAC CHORI RRID : NA RP23–329L1 - eGFP-L10a This paper Cacng5-bacTRAP - modified BAC , RRID : NA RP23–181A2 - eGFP-L10a This paper Calca-bacTRAP - modified BAC , RRID : NA RP24–68J22- eGFP-L10a This paper Cartpt - modified BAC , RRID : NA RP23–307B16 - eGFP-L10a This paper Sh3bgrl2-bacTRAP - modified BAC , RRID : NA RP23–199D5 - eGFP-L10a This paper Rasgrp2–199D5-bacTRAP - modified BAC, RRID : NA RP24–344N1 - eGFP-L10a This paper Rasgrp2–344N1-bacTRAP – modified BAC, RRID : NA RP23–126C5 - eGFP-L10a This paper Sstr4-bacTRAP - modified BAC , RRID : NA mouse Ptbp1 untagged cDNA clone {"type":"entrez-nucleotide","attrs":{"text":"NM_008956","term_id":"545687870"}} NM_008956 Origene Cat# {"type":"entrez-nucleotide","attrs":{"text":"MG223224","term_id":"1316024794"}} MG223224 , RRID : NA Software and Algorithms htseq Anders et al., 2015 https://github.com/htseq/htseq FIMO Grant et al., 2011 http://meme-suite.org/doc/fimo.html edgeR Robinson et al., 2010 http://bioconductor.org/packages/devel/bioc/html/edgeR.html The Sleipnir Library for Computational Functional Genomics Huttenhower et al., 2008 https://libsleipnir.bitbucket.io/ VEGAS2 Mishra and Macgregor, 2015 https://vegas2.qimrberghofer.edu.au/ STAR Dobin et al., 2013 https://github.com/alexdobin/STAR Open in a separate window KEY RESOURCES TABLE

Techniques: Immunofluorescence, Plasmid Preparation, shRNA, Sequencing, Expressing, Functional Assay, Over Expression, Purification, Recombinant, Modification, BAC Assay, Software

(A) RNA ploy II ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). (B) Left: western blot analysis of PTBP1 in hLMR1 pulldown, right: expression of hLMR1 in PTBP1 RIP (RNA immunoprecipitation) in humanized liver. (C) HMGCS1 promoter-driven luciferase reporter assay in 293A cells (n=3 for each group). Data are representative results of three independent experiments. (D) PTBP1 ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). Error bars represent SEM, * p<0.05.

Journal: bioRxiv

Article Title: Multilevel integrative transcriptome analyses in humans and humanized mice define in vivo human lncRNA metabolic regulators

doi: 10.1101/2020.01.01.884023

Figure Lengend Snippet: (A) RNA ploy II ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). (B) Left: western blot analysis of PTBP1 in hLMR1 pulldown, right: expression of hLMR1 in PTBP1 RIP (RNA immunoprecipitation) in humanized liver. (C) HMGCS1 promoter-driven luciferase reporter assay in 293A cells (n=3 for each group). Data are representative results of three independent experiments. (D) PTBP1 ChIP analyses in liver tissues of humanized mice receiving adenovirus for control (sh-lacZ, n=3) or knocking down of hLMR1 (sh-hLMR1, n=3). Error bars represent SEM, * p<0.05.

Article Snippet: Full-length PTBP1 expression vector and control vector were purchased from OriGene (Cat: RC201779 and PS100001).

Techniques: Western Blot, Expressing, Immunoprecipitation, Luciferase, Reporter Assay

(A) Gene expression in the liver of regular mice receiving lacZ shRNA (sh-lacZ, n=9), or shRNA for Ptbp1 (sh-Ptbp1, n=7). (B) Gene expression in the liver of regular mice receiving adenovirus for control (Ad-Vector, n=5) or expression of hLMR1 (Ad-hLMR1, n=6). (C) Plasma (left) and liver (right) cholesterol levels in regular mice receiving adenovirus for control (Ad-Vector, n=9) or expressing of hLMR1 (Ad-hLMR1, n=9). Error bars represent SEM, * p<0.05.

Journal: bioRxiv

Article Title: Multilevel integrative transcriptome analyses in humans and humanized mice define in vivo human lncRNA metabolic regulators

doi: 10.1101/2020.01.01.884023

Figure Lengend Snippet: (A) Gene expression in the liver of regular mice receiving lacZ shRNA (sh-lacZ, n=9), or shRNA for Ptbp1 (sh-Ptbp1, n=7). (B) Gene expression in the liver of regular mice receiving adenovirus for control (Ad-Vector, n=5) or expression of hLMR1 (Ad-hLMR1, n=6). (C) Plasma (left) and liver (right) cholesterol levels in regular mice receiving adenovirus for control (Ad-Vector, n=9) or expressing of hLMR1 (Ad-hLMR1, n=9). Error bars represent SEM, * p<0.05.

Article Snippet: Full-length PTBP1 expression vector and control vector were purchased from OriGene (Cat: RC201779 and PS100001).

Techniques: Expressing, shRNA, Plasmid Preparation

gRNA-dependent off-target binding alters the expression of essential genes and induces substantial alterations in cell proliferation. ( A – D ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the PspCas13b-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. ( E – H ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the RfxCas13d-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. RT-qPCR data are presented as mean ± SD ( n = 3). Relative changes in protein abundance were quantified by densitometric analysis and are indicated as red numbers at the bottom of each panel. ( I ) Proliferation of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or a non-targeting control gRNA (gNT), measured by CCK-8 assay. Proliferation rates were measured by absorbance at days 1–5 and normalized to that at day 1. Data are presented as mean ± SD ( n = 4). * P < 0.05; ** P < 0.01; *** P < 0.001. ns, not significant. ( J ) Apoptosis analysis of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or non-targeting control gRNA (gNT). Data are presented as mean ± SD ( n = 3). ns, not significant.

Journal: Nucleic Acids Research

Article Title: Characterization of gRNA-dependent and gRNA-independent off-target binding sites of PspCas13b and RfxCas13d in mammalian cells

doi: 10.1093/nar/gkag112

Figure Lengend Snippet: gRNA-dependent off-target binding alters the expression of essential genes and induces substantial alterations in cell proliferation. ( A – D ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the PspCas13b-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. ( E – H ) RT-qPCR and western blot analyses of on-target EZH2 and three gRNA-dependent off-target genes bound by the RfxCas13d-EZH2-g2 complex, with comparisons between non-targeting and EZH2-g2 targeting conditions. RT-qPCR data are presented as mean ± SD ( n = 3). Relative changes in protein abundance were quantified by densitometric analysis and are indicated as red numbers at the bottom of each panel. ( I ) Proliferation of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or a non-targeting control gRNA (gNT), measured by CCK-8 assay. Proliferation rates were measured by absorbance at days 1–5 and normalized to that at day 1. Data are presented as mean ± SD ( n = 4). * P < 0.05; ** P < 0.01; *** P < 0.001. ns, not significant. ( J ) Apoptosis analysis of cells expressing PspCas13b (left panel) or RfxCas13d (right panel) with either targeting gRNAs or non-targeting control gRNA (gNT). Data are presented as mean ± SD ( n = 3). ns, not significant.

Article Snippet: The following antibodies were used for western blot analysis in this study: PTBP1 polyclonal antibody (Proteintech, 12582-1-AP), RHOA polyclonal antibody (Proteintech, 10749-1-AP), CTSH polyclonal antibody (Proteintech, 10315-1-AP), CDK19 polyclonal antibody (Proteintech, 13761-1-AP), HMGN2 polyclonal antibody (Proteintech, 10953-1-AP), ACVR2B antibody (Abmart, T58048 ), NUCKS1 polyclonal antibody (Proteintech, 12023-2-AP), HMGA1 polyclonal antibody (Proteintech, 29895-1-AP), EZH2 polyclonal antibody (Proteintech, 21800-1-AP), EFNA3 polyclonal antibody (Proteintech, 12480-1-AP), HPSE polyclonal antibody (Proteintech, 24529-1-AP), SPG7 polyclonal antibody (Proteintech, 27801-1-AP), TRAF3 polyclonal antibody (Proteintech, 18099-1-AP), MDK polyclonal antibody (Proteintech, 11009-1-AP), SCRN1 polyclonal antibody (Proteintech, 14303-1-AP), HA-Tag (26D11) mAb (Abmart, M20003L), GAPDH (3B3) mAb (Abmart, M20006L), ACSL1 polyclonal antibody (Proteintech, 13989-1-AP), FASN polyclonal antibody (Proteintech, 10624-2-AP), RPL14 polyclonal antibody (Proteintech, 14991-1-AP), ACOX1 polyclonal antibody (Proteintech, 10957-1-AP), ACO2 polyclonal antibody (Proteintech, 11134-1-AP), EIF2D polyclonal antibody (Proteintech, 12840-1-AP).

Techniques: Binding Assay, Expressing, Quantitative RT-PCR, Western Blot, Quantitative Proteomics, Control, CCK-8 Assay