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cancer antigen 125 ca 125  (HyTest)


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    Structured Review

    HyTest cancer antigen 125 ca 125
    Selectivity studies using a competitive method between the target molecule and the interfering species. The interfering species studied were CEA, CA 125, and urea.
    Cancer Antigen 125 Ca 125, supplied by HyTest, used in various techniques. Bioz Stars score: 96/100, based on 19 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ca/CA-125/pmc11089526-62-95-101
    Average 96 stars, based on 19 article reviews
    cancer antigen 125 ca 125 - by Bioz Stars, 2026-10
    96/100 stars

    Images

    1) Product Images from "An electrochemically synthesized molecularly imprinted polymer for highly selective detection of breast cancer biomarker CA 15-3: a promising point-of-care biosensor † "

    Article Title: An electrochemically synthesized molecularly imprinted polymer for highly selective detection of breast cancer biomarker CA 15-3: a promising point-of-care biosensor †

    Journal: RSC Advances

    doi: 10.1039/d4ra02051k

    Selectivity studies using a competitive method between the target molecule and the interfering species. The interfering species studied were CEA, CA 125, and urea.
    Figure Legend Snippet: Selectivity studies using a competitive method between the target molecule and the interfering species. The interfering species studied were CEA, CA 125, and urea.

    Techniques Used:

    Related Articles

    Isolation:

    Article Title: Immunosensing Cancer Markers through Surface-Enhanced Photoluminescence on Nanostructured Silver Substrates
    Article Snippet: The silver nitrate (AgNO3; purity ≥ 99.0%) was from Sigma-Aldrich (Taufkirchen, Germany). .. Human cancer antigen 125 (CA125) isolated from human adenocarcinoma (250 kIU) was obtained from HyTest (Turku, Finland). .. Recombinant human epididymis protein 4 antigen (100 μg; purity ≥ 85%) was from EastCoast Bio (Maryland Heights, MO, USA).

    other:

    Article Title: Role of Defects of Carbon Nanomaterials in the Detection of Ovarian Cancer Cells in Label-Free Electrochemical Immunosensors.
    Article Snippet: Ab (X306) was purchased from HyTest Ltd., (Turku, Finland), and Ag (CA125) was purchased from purchased from Bio-techne, (Minneapolis, MN, USA).

    Recombinant:

    Article Title: Intelligent POCT for ovarian cancer: Dual-biomarker detection combined with ROMA risk assessment using selenium nanoparticle
    Article Snippet: The early diagnosis of ovarian cancer remains dissolved due to the lack of detection methods that are sensitive, rapid and accessible.. To address this clinical challenge, this study developed an innovative diagnostic platform integrating a novel selenium nanoparticles (SeNPs) probe, dual-biomarker (CA125 and HE4) detection and intelligent analysis system.. The detection limits for CA125 and HE4 were determined to be 35 U/mL and 100 pmol/L respectively, and no cross-reactivity was observed.

    Saline:

    Article Title: An Innovative Approach for Tailoring Molecularly Imprinted Polymers for Biosensors—Application to Cancer Antigen 15-3
    Article Snippet: Metallic copper (Cu 0 wire, d = 1 mm, Sigma Aldrich) was washed with HCl in methanol and subsequently rinsed with methanol and dried under a stream of nitrogen, following procedures in the literature [ ]. .. The electrochemical assays used potassium hexacyanoferrate III (K 3 [Fe(CN) 6 ]) and potassium hexacyanoferrate II (K 4 [Fe(CN) 6 ]) trihydrate obtained from Riedel-de Häen (Seelze, Germany); N -hydroxysuccinimide (NHS) and oxalic acid obtained from Merk (Darmstadt, Germany); N -(3-dimethyl aminopropyl)- N ′-ethyl-carbodiimide hydrochloride (EDAC), 3-mercaptopropionic acid (3-MPA), proteinase K, and 2-aminoethyl methacrylate hydrochloride (AMA) obtained from Sigma-Aldrich; a phosphate-buffered saline (PBS, 0.01 M, pH 7.4) solution obtained from Panreac (Barcelona, Spain); fetal bovine serum (FBS) and glucose obtained from Alfa Aesar; urea obtained from Fagron (Rotterdam, The Netherlands); sulphuric acid (H 2 SO 4 ) obtained from BDH (Providence, RI, USA); 2-( N -morpholino)ethanosulfonic acid (MES) from AppliChem (Darmstadt, Germany); carcinoembryonic antigen (CEA), 25 μg, from EastCoastBio (North Berwick, ME, USA); CA 125, 250 kU, from Hytest (Turku, Finland); and CA 15-3, 17,420 U/mL, from EmelcaBioScience (Clinge, The Netherlands). ..

    Article Title: SERS biosensor with plastic antibodies for detection of a cancer biomarker protein
    Article Snippet: All chemicals were of analytical grade and the water was ultra-pure Milli-Q laboratory water. .. Potassium ferricyanide II-3-hydrate (K 4 Fe(CN) 6 ∙3H 2 O) and potassium ferricyanide III (K 3 Fe(CN) 6 ) were purchased from Riedel de Haën; N,N-dimethylformamide (DMF) (C 3 H7NO), tri-sodium citrate dihydrate (C 6 H 5 Na 3 O 7∙ 2H 2 O), and aniline (C 6 H 7 N) were purchased from Analar Normapur; ethanol absolute (C 2 H 5 OH) ≥ 99.9%, hydrotetrachloric acid (HAuCl4∙3H 2 O), trypsin, and polyvinylpyrrolidone (PVP, (C 6 H 9 NO)n) with a molecular weight of 10,000 were purchased from Sigma-Aldrich; 4-ATP (C 6 H 7 NS) ≥ 97% was purchased from Merck; glucose was purchased from Alfa Aesar; hydrochloric acid (HCl) 37%, nitric acid (HNO 3 ) 70%, and phosphate-buffered saline (PBS, 0.01 M, pH 7.4) were purchased from Panreac; sulfuric acid (H 2 SO 4 ) was purchased from BDH; SDS was purchased from TCI; CORMAY serum HN was purchased from Cormay®; carcinoembryonic antigen was purchased from EastCostBio; cancer antigen 125 (CA-125) was purchased from Hytest; CA 15–3 from human host (reference MBS536585) was purchased from MyBioSource; CA 15–3 antibody (mucin 1 monoclonal antibody Vu-2G7, reference SC-69644) was purchased from Santa Cruz Biotechnology. ..

    Molecular Weight:

    Article Title: SERS biosensor with plastic antibodies for detection of a cancer biomarker protein
    Article Snippet: All chemicals were of analytical grade and the water was ultra-pure Milli-Q laboratory water. .. Potassium ferricyanide II-3-hydrate (K 4 Fe(CN) 6 ∙3H 2 O) and potassium ferricyanide III (K 3 Fe(CN) 6 ) were purchased from Riedel de Haën; N,N-dimethylformamide (DMF) (C 3 H7NO), tri-sodium citrate dihydrate (C 6 H 5 Na 3 O 7∙ 2H 2 O), and aniline (C 6 H 7 N) were purchased from Analar Normapur; ethanol absolute (C 2 H 5 OH) ≥ 99.9%, hydrotetrachloric acid (HAuCl4∙3H 2 O), trypsin, and polyvinylpyrrolidone (PVP, (C 6 H 9 NO)n) with a molecular weight of 10,000 were purchased from Sigma-Aldrich; 4-ATP (C 6 H 7 NS) ≥ 97% was purchased from Merck; glucose was purchased from Alfa Aesar; hydrochloric acid (HCl) 37%, nitric acid (HNO 3 ) 70%, and phosphate-buffered saline (PBS, 0.01 M, pH 7.4) were purchased from Panreac; sulfuric acid (H 2 SO 4 ) was purchased from BDH; SDS was purchased from TCI; CORMAY serum HN was purchased from Cormay®; carcinoembryonic antigen was purchased from EastCostBio; cancer antigen 125 (CA-125) was purchased from Hytest; CA 15–3 from human host (reference MBS536585) was purchased from MyBioSource; CA 15–3 antibody (mucin 1 monoclonal antibody Vu-2G7, reference SC-69644) was purchased from Santa Cruz Biotechnology. ..



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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), <t>CA074</t> (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).
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    Image Search Results


    Limit of Detection of different HPV genotypes on the Steripack XpressCollect flocked nylon swab on the Atila ScreenFire HPV RS assay.

    Journal: Gates Open Research

    Article Title: Analytical performance and clinical usability of a low-cost vaginal swab for sensitive detection of high-risk human papillomavirus

    doi: 10.12688/gatesopenres.16399.1

    Figure Lengend Snippet: Limit of Detection of different HPV genotypes on the Steripack XpressCollect flocked nylon swab on the Atila ScreenFire HPV RS assay.

    Article Snippet: Human cervical cancer cell lines including SiHa (ATCC HTB-35), HeLa (ATCC CCL-2), CaSki (ATCC CRL-1550), and C-33A (ATCC HTB-31) cells from American Type Culture Collection (ATCC, Manassas, VA, USA) were grown at 37°C with 5% CO 2 in culture media: Dulbecco’s Modified Eagle Medium high glucose with sodium pyruvate containing 10% Fetal Bovine Serum (Gibco, Thermo Fisher Scientific, Waltham, MA, USA) and 50 μg/mL gentamycin (Sigma-Aldrich, St. Louis, MO, USA) under standard aseptic conditions while screening for mycoplasma contamination using the Universal Mycoplasma Detection kit (ATCC, Manassas, VA, USA) according to the manufacturer’s instructions.

    Techniques: Plasmid Preparation

    ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), CA074 (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).

    Journal: Science Advances

    Article Title: Phosphorylation by CaMKIV regulates the transcriptional repressor activity and half-life of REST/NRSF

    doi: 10.1126/sciadv.aec0781

    Figure Lengend Snippet: ( A ) Schematics of the four possible degradation pathways that CaMKIV-phosphorylated REST can undertake and the three inhibitors that were used to dissect the fate of REST. Cat, cathepsin. ( B ) HEK293T cells were transfected with WT, CA, or KD CaMKIV and treated with cycloheximide (CHX) to in4hibit further translation. Then, cells were treated for 16 hours with either vehicle [dimethyl sulfoxide (DMSO)] or MG-132 (5 μM), an inhibitor of the ubiquitin-proteasome system (UPS). Left: Representative immunoblots monitoring the expression of WT, CA, and KD CaMKs, REST, and calnexin, respectively, in HEK293T cells, 48 hours after transfection with the kinase constructs. Right: Mean (±SEM) REST protein levels, shown as ratios with calnexin immunoreactivity under the various experimental conditions. No effects of inhibition of the UPS were observed. * P = 0.017, CA versus WT in DMSO; ** P = 0.0048, CA versus WT in MG-132. Two-way ANOVA/Tukey’s tests ( n = 4 independent preparations). ( C ) HEK293T cells were transfected with either WT or CA CaMKIV and treated with CHX to inhibit further translation. Successively, cells were treated for 16 hours with DMSO (Veh), bafilomycin A1 (Baf; 100 nM; an inhibitor of lysosomal acidification and autophagy), leupeptin (Leu; 40 μM; an inhibitor of the lysosomal and cytosolic proteases), CA074 (a specific inhibitor of Cathepsin B), or E64 (an inhibitor of cathepsins). Left: Representative immunoblots monitoring the expression of REST, calnexin, and the autophagy markers p62 and LC3B-I and -II. Right: Mean (±SEM) REST/calnexin ratios normalized with respect to the control REST/calnexin ratio in WT CaMKIV–expressing cells. Leu, * P = 0.0351; CA074, * P = 0.0361; E64, * P = 0.0481. Mixed-effects ANOVA/Dunnett’s tests ( n = 4 independent preparations).

    Article Snippet: W7, KN92, KN93, CA074, E64, bicuculline, CGP58845 , d -aminophosphovalerate, and tetrodotoxin were from Tocris (Bristol, UK).

    Techniques: Transfection, Ubiquitin Proteomics, Western Blot, Expressing, Construct, Inhibition, Control