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human ccl14 elisa kit  (Boster Bio)


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    Boster Bio human ccl14 elisa kit
    Human Ccl14 Elisa Kit, supplied by Boster Bio, 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/human+ccl14+elisa+kit/Human+CCL14+ELISA+Kit+EZ-Set/pm41559739-94-12-16
    Average 94 stars, based on 1 article reviews
    human ccl14 elisa kit - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: CCL14, identified by multi-omics approach, serves as a novel indicator of disease severity and progression in lymphangioleiomyomatosis
    Article Snippet: Serum concentrations of VEGF-D in samples from 53 disease subjects and 25 healthy controls were quantified using a human VEGF-D ELISA kit (R&D Systems, USA). .. Plasma concentrations of CCL14 in the same cohort were measured using a human CCL14 ELISA kit (Boster Biological Technology, China). ..

    Article Title: CCL14, identified by multi-omics approach, serves as a novel indicator of disease severity and progression in lymphangioleiomyomatosis.
    Article Snippet: Serum concentrations of VEGF-D in samples from 53 disease subjects and 25 healthy controls were quantified using a human VEGF-D ELISA kit (R&D Systems, USA). .. Plasma concentrations of CCL14 in the same cohort were measured using a human CCL14 ELISA kit (Boster Biological Technology, China). ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: CCL14, identified by multi-omics approach, serves as a novel indicator of disease severity and progression in lymphangioleiomyomatosis
    Article Snippet: Serum concentrations of VEGF-D in samples from 53 disease subjects and 25 healthy controls were quantified using a human VEGF-D ELISA kit (R&D Systems, USA). .. Plasma concentrations of CCL14 in the same cohort were measured using a human CCL14 ELISA kit (Boster Biological Technology, China). ..

    Article Title: CCL14, identified by multi-omics approach, serves as a novel indicator of disease severity and progression in lymphangioleiomyomatosis.
    Article Snippet: Serum concentrations of VEGF-D in samples from 53 disease subjects and 25 healthy controls were quantified using a human VEGF-D ELISA kit (R&D Systems, USA). .. Plasma concentrations of CCL14 in the same cohort were measured using a human CCL14 ELISA kit (Boster Biological Technology, China). ..



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    Urinary biomarkers levels on day 0 stratified by renal recovery. Day 0 means the day of AKI diagnosis . TIMP-2 tissue inhibitor of metalloproteinases-2, IGFBP-7 insulin-like growth factor-binding protein 7, <t>CCL14</t> C–C motif chemokine ligand 14, NGAL neutrophil gelatinase-associated lipocalin
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    AXL/SOX2/DKK-1 axis in HUVECs promotes HCC metastasis. (A) DKK-1 and <t>CCL14</t> secretion was significantly downregulated in CM from HUVEC-AXL-KD compared with that from HUVEC-AXL-NC, as detected with a human cytokine antibody array. (B) DKK-1 and CCL14 expression was markedly upregulated in the CM of HUVECs overexpressing AXL (CCL14: p < 0.001; DKK-1: p = 0.003) compared with the CM of HUVEC-AXL-NC, as detected by <t>ELISA</t> assay. (C) AXL siRNA downregulated DKK-1 and CCL14 secretion in the CM of HUVEC-AXL-NC and HUVEC-AXL-OE cells (CCL14: p < 0.001 and p < 0.001; DKK-1: p < 0.001 and p < 0.001). (D) DKK1 siRNA (MHCC-97L: p < 0.001 and p < 0.001; HCC-LM3: p <0.001 and p < 0.001), but not CCL14 siRNA (MHCC-97L: p = 0.126 and p = 0.711; HCC-LM3: p = 0.901 and p = 0.694) could attenuate the effect of the CM from HUVEC-AXL-NC and HUVEC-AXL-OE cells on the migration of HCC-LM3 cells and MHCC-97L cells. (E) SOX2 mRNA expression was significantly increased in HUVEC-AXL-OE cells and decreased in HUVEC-AXL-KD cells compared with HUVEC-AXL-NC cells (HUVEC-AXL-KD: p < 0.001, HUVEC-AXL-OE: p < 0.001). (F) AXL overexpression could significantly increase SOX2 and DKK-1 protein expression in HUVEC-AXL-OE cells compared with HUVEC-AXL-NC cells, and SOX2 siRNA inhibited SOX2 and DKK-1 protein expression in HUVEC-AXL-OE and HUVEC-AXL-NC cells.
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    Image Search Results


    Urinary biomarkers levels on day 0 stratified by renal recovery. Day 0 means the day of AKI diagnosis . TIMP-2 tissue inhibitor of metalloproteinases-2, IGFBP-7 insulin-like growth factor-binding protein 7, CCL14 C–C motif chemokine ligand 14, NGAL neutrophil gelatinase-associated lipocalin

    Journal: Journal of Intensive Care

    Article Title: Analysis of urinary C–C motif chemokine ligand 14 (CCL14) and first-generation urinary biomarkers for predicting renal recovery from acute kidney injury: a prospective exploratory study

    doi: 10.1186/s40560-023-00659-2

    Figure Lengend Snippet: Urinary biomarkers levels on day 0 stratified by renal recovery. Day 0 means the day of AKI diagnosis . TIMP-2 tissue inhibitor of metalloproteinases-2, IGFBP-7 insulin-like growth factor-binding protein 7, CCL14 C–C motif chemokine ligand 14, NGAL neutrophil gelatinase-associated lipocalin

    Article Snippet: NGAL and CCL14 were measured by enzyme-linked immunosorbent assay (ab119600 (NGAL); ab272201 (CCL14), Abcam, UK).

    Techniques: Biomarker Discovery, Binding Assay

    Predictive accuracy of urinary biomarkers on day 0 for renal non-recovery

    Journal: Journal of Intensive Care

    Article Title: Analysis of urinary C–C motif chemokine ligand 14 (CCL14) and first-generation urinary biomarkers for predicting renal recovery from acute kidney injury: a prospective exploratory study

    doi: 10.1186/s40560-023-00659-2

    Figure Lengend Snippet: Predictive accuracy of urinary biomarkers on day 0 for renal non-recovery

    Article Snippet: NGAL and CCL14 were measured by enzyme-linked immunosorbent assay (ab119600 (NGAL); ab272201 (CCL14), Abcam, UK).

    Techniques:

    ROC curves of clinical model and corresponding urinary biomarkers model on day 0 for predicting renal non-recovery. Day 0 means the day of AKI diagnosis. a Compared with clinical model. Clinical model included non-renal SOFA score and AKI stage. AUC area under the receiver operating characteristics curve, CCL14 C–C motif chemokine ligand 14, TIMP-2 tissue inhibitor of metalloproteinases-2, IGFBP-7 insulin-like growth factor-binding protein 7

    Journal: Journal of Intensive Care

    Article Title: Analysis of urinary C–C motif chemokine ligand 14 (CCL14) and first-generation urinary biomarkers for predicting renal recovery from acute kidney injury: a prospective exploratory study

    doi: 10.1186/s40560-023-00659-2

    Figure Lengend Snippet: ROC curves of clinical model and corresponding urinary biomarkers model on day 0 for predicting renal non-recovery. Day 0 means the day of AKI diagnosis. a Compared with clinical model. Clinical model included non-renal SOFA score and AKI stage. AUC area under the receiver operating characteristics curve, CCL14 C–C motif chemokine ligand 14, TIMP-2 tissue inhibitor of metalloproteinases-2, IGFBP-7 insulin-like growth factor-binding protein 7

    Article Snippet: NGAL and CCL14 were measured by enzyme-linked immunosorbent assay (ab119600 (NGAL); ab272201 (CCL14), Abcam, UK).

    Techniques: Biomarker Discovery, Binding Assay

    NRI and IDI for assessing the contributions of different biomarkers for non-recovery prediction when combing with clinical model

    Journal: Journal of Intensive Care

    Article Title: Analysis of urinary C–C motif chemokine ligand 14 (CCL14) and first-generation urinary biomarkers for predicting renal recovery from acute kidney injury: a prospective exploratory study

    doi: 10.1186/s40560-023-00659-2

    Figure Lengend Snippet: NRI and IDI for assessing the contributions of different biomarkers for non-recovery prediction when combing with clinical model

    Article Snippet: NGAL and CCL14 were measured by enzyme-linked immunosorbent assay (ab119600 (NGAL); ab272201 (CCL14), Abcam, UK).

    Techniques:

    AXL/SOX2/DKK-1 axis in HUVECs promotes HCC metastasis. (A) DKK-1 and CCL14 secretion was significantly downregulated in CM from HUVEC-AXL-KD compared with that from HUVEC-AXL-NC, as detected with a human cytokine antibody array. (B) DKK-1 and CCL14 expression was markedly upregulated in the CM of HUVECs overexpressing AXL (CCL14: p < 0.001; DKK-1: p = 0.003) compared with the CM of HUVEC-AXL-NC, as detected by ELISA assay. (C) AXL siRNA downregulated DKK-1 and CCL14 secretion in the CM of HUVEC-AXL-NC and HUVEC-AXL-OE cells (CCL14: p < 0.001 and p < 0.001; DKK-1: p < 0.001 and p < 0.001). (D) DKK1 siRNA (MHCC-97L: p < 0.001 and p < 0.001; HCC-LM3: p <0.001 and p < 0.001), but not CCL14 siRNA (MHCC-97L: p = 0.126 and p = 0.711; HCC-LM3: p = 0.901 and p = 0.694) could attenuate the effect of the CM from HUVEC-AXL-NC and HUVEC-AXL-OE cells on the migration of HCC-LM3 cells and MHCC-97L cells. (E) SOX2 mRNA expression was significantly increased in HUVEC-AXL-OE cells and decreased in HUVEC-AXL-KD cells compared with HUVEC-AXL-NC cells (HUVEC-AXL-KD: p < 0.001, HUVEC-AXL-OE: p < 0.001). (F) AXL overexpression could significantly increase SOX2 and DKK-1 protein expression in HUVEC-AXL-OE cells compared with HUVEC-AXL-NC cells, and SOX2 siRNA inhibited SOX2 and DKK-1 protein expression in HUVEC-AXL-OE and HUVEC-AXL-NC cells.

    Journal: Frontiers in Oncology

    Article Title: AXL Overexpression in Tumor-Derived Endothelial Cells Promotes Vessel Metastasis in Patients With Hepatocellular Carcinoma

    doi: 10.3389/fonc.2021.650963

    Figure Lengend Snippet: AXL/SOX2/DKK-1 axis in HUVECs promotes HCC metastasis. (A) DKK-1 and CCL14 secretion was significantly downregulated in CM from HUVEC-AXL-KD compared with that from HUVEC-AXL-NC, as detected with a human cytokine antibody array. (B) DKK-1 and CCL14 expression was markedly upregulated in the CM of HUVECs overexpressing AXL (CCL14: p < 0.001; DKK-1: p = 0.003) compared with the CM of HUVEC-AXL-NC, as detected by ELISA assay. (C) AXL siRNA downregulated DKK-1 and CCL14 secretion in the CM of HUVEC-AXL-NC and HUVEC-AXL-OE cells (CCL14: p < 0.001 and p < 0.001; DKK-1: p < 0.001 and p < 0.001). (D) DKK1 siRNA (MHCC-97L: p < 0.001 and p < 0.001; HCC-LM3: p <0.001 and p < 0.001), but not CCL14 siRNA (MHCC-97L: p = 0.126 and p = 0.711; HCC-LM3: p = 0.901 and p = 0.694) could attenuate the effect of the CM from HUVEC-AXL-NC and HUVEC-AXL-OE cells on the migration of HCC-LM3 cells and MHCC-97L cells. (E) SOX2 mRNA expression was significantly increased in HUVEC-AXL-OE cells and decreased in HUVEC-AXL-KD cells compared with HUVEC-AXL-NC cells (HUVEC-AXL-KD: p < 0.001, HUVEC-AXL-OE: p < 0.001). (F) AXL overexpression could significantly increase SOX2 and DKK-1 protein expression in HUVEC-AXL-OE cells compared with HUVEC-AXL-NC cells, and SOX2 siRNA inhibited SOX2 and DKK-1 protein expression in HUVEC-AXL-OE and HUVEC-AXL-NC cells.

    Article Snippet: The protein concentrations of CCL14 and DKK-1 in the supernatants were also measured using an enzyme-linked immunosorbent assay (ELISA) kit (CCL14: EK1123 Boster, Wuhan, China; DKK-1: EK0867 Boster, Wuhan, China) according to the manufacturer’s instructions.

    Techniques: Ab Array, Expressing, Enzyme-linked Immunosorbent Assay, Migration, Over Expression