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Human IGFBP7 ELISA Kit für Sandwich ELISA - ABIN5596293
Nakamura, Hosoyama, Kawamura, Takeuchi, Tanaka, Samura, Ueno, Nishimoto, Kurazumi, Suzuki, Ito, Sakata, Mikamo, Li, Hamano: Influence of aging on the quantity and quality of human cardiac stem cells. in Scientific reports 2016
Human IGFBP7 ELISA Kit für Sandwich ELISA - ABIN1081560
Watanabe, Takiyama, Honjyo, Makino, Fujita, Tateno, Haneda: Role of IGFBP7 in Diabetic Nephropathy: TGF-β1 Induces IGFBP7 via Smad2/4 in Human Renal Proximal Tubular Epithelial Cells. in PLoS ONE 2016
epithelial cells and leukocytes from the urinary sediment. CONCLUSION: The gene expression pattern of IGFBP7 and TIMP-2 (zeige TIMP2 ELISA Kits) from urinary sediment, which contains desquamated renal tubular epithelial cells, did not correlate with [IGFBP7]x[TIMP-2 (zeige TIMP2 ELISA Kits)] protein, indicating that IGFBP7 and TIMP-2 (zeige TIMP2 ELISA Kits) measured in the NephroCheck(R) test originated predominantly from intact but stressed cells of the kidney itself
In patients with heart failure with preserved ejection fraction, IGFBP7 may be a novel biomarker of diastolic function and exercise capacity.
High IGFBP7 expression is associated with acute kidney injury.
NEAT1-associated paraspeckle proteins P54nrb (zeige NONO ELISA Kits) and PSF have been reported as positive regulators of c-Myc (zeige MYC ELISA Kits) translation through interaction with c-Myc (zeige MYC ELISA Kits) IRES
Urine [TIMP-2 (zeige TIMP2 ELISA Kits)]*[IGFBP7] is a promising candidate for early detection of AKI, especially in ruling-out AKI
Meta-analysis indicated that urinary [TIMP-2 (zeige TIMP2 ELISA Kits)].[IGFBP7] may be a reliable biomarker for the early detection of acute kidney injury in adults.
TIMP-2 (zeige TIMP2 ELISA Kits) is both expressed and secreted preferentially by cells of distal tubule origin, while IGFBP7 is equally expressed across tubule cell types yet preferentially secreted by cells of proximal tubule origin. In human kidney tissue, strong staining of IGFBP7 was seen in the luminal brush-border region of a subset of proximal tubule cells, and TIMP-2 (zeige TIMP2 ELISA Kits) stained intracellularly in distal tubules.
loss of IGFBP7 and upregulation of IGF1 (zeige IGF1 ELISA Kits) activates the FGF4 (zeige FGF4 ELISA Kits)-FGFR1 (zeige FGFR1 ELISA Kits)-ETS2 (zeige ETS2 ELISA Kits) pathway in Tumor-associated endothelial cells (TECs) and converts naive tumor cells to chemoresistant tumor stem-like cells (TSCs), thereby facilitating their invasiveness and progression.
Data report that IGFBP7 is a novel target gene of ADAR2 (zeige ADARB1 ELISA Kits) in esophageal squamous cell carcinoma where its RNA is edited and protein stabilized by ADAR2 (zeige ADARB1 ELISA Kits).
analysis of how A-to-I RNA editing of the IGFBP7 transcript increases during aging in porcine brain tissues
Our findings define an immune component of the pleiotropic mechanisms through which IGFBP7 suppresses hepatocellular carcinoma
Study shows that IGFBP7 contributes significantly to mesenchymal stromal cells (MSC (zeige MSC ELISA Kits))-mediated immune modulation, as is shown by decreasing ability of IGFBP7 knockdown in MSCs to restore proliferation and cytokine production in T-cells.
data suggest that IGFBP-7 was up regulated during EAE and inhibit the transition from OPCs to mature OLs, implying its use as a potential therapeutic target for the treatment of inflammatory demyelinating diseases
Our data suggest that loss of Igfbp7 induces precocious involution possibly through diminished cell survival signals.
Angiomodulin is necessary for cardiac commitment of embryonic stem cells (ESCs (zeige NR2E3 ELISA Kits)) and its regulation depends on TAp63 isoform.
results show that Smarcb1 (zeige SMARCB1 ELISA Kits) is required for transcriptional activation of Igfbp7 and show that re-introduction of Igfbp7 alone can hinder tumor development; results define a novel mechanism for Smarcb1 (zeige SMARCB1 ELISA Kits)-mediated tumorigenesis
a model whereby IGFBP7 binds to unoccupied IGF1R (zeige IGF1R ELISA Kits) and suppresses downstream signaling, thereby inhibiting protein synthesis, cell growth, and survival.
IGFBP7 has a novel role in mouse uterus: it is regulating uterine receptivity through Th1 (zeige HAND1 ELISA Kits)/Th2 lymphocyte balance and decidualization.
fear extinction-induced IGF2/IGFBP7 signalling promotes the survival of 17-19-day-old newborn hippocampal neurons
Results demonstrate that the vascular-specific marker angiomodulin (AGM) modulates vascular remodeling in part by temporizing the proangiogenic effects of VEGF-A (zeige VEGFA ELISA Kits).
This gene encodes a member of the insulin-like growth factor (IGF)-binding protein (IGFBP) family. IGFBPs bind IGFs with high affinity, and regulate IGF availability in body fluids and tissues and modulate IGF binding to its receptors. This protein binds IGF-I and IGF-II with relatively low affinity, and belongs to a subfamily of low-affinity IGFBPs. It also stimulates prostacyclin production and cell adhesion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene, and one variant has been associated with retinal arterial macroaneurysm (PMID:21835307).
insulin-like growth factor-binding protein 7
, IGF-binding protein 7
, PGI2-stimulating factor
, prostacyclin-stimulating factor
, tumor-derived adhesion factor