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Human KIT ELISA Kit for Sandwich ELISA - ABIN414919
Suh, Chon, Choi: Protective effects of honokiol against methylglyoxal-induced osteoblast damage. in Chemico-biological interactions 2016
the critical physiological role of the KIT-ET3 (show EDN3 ELISA Kits)-NO pathway in fulfilling high demand (exceeding basal level) of endothelium-dependent NO generation for coping with atherosclerosis, pregnancy, and aging, is reported.
determined that miR (show MLXIP ELISA Kits)-137 can participate in the leukemogenesis by regulating c-kit, which could be used as a therapeutic target for acute myeloid leukemia (show BCL11A ELISA Kits)
Report up-regulation of the mTOR (show FRAP1 ELISA Kits), PDGF (show PDGFA ELISA Kits), VEGF (show VEGFA ELISA Kits), and c-kit pathways in a large cohort of Kaposi sarcoma samples.
c-KIT overexpressing cells showed a regression of typical morphological features of malignancy. Taken together these results suggest that c-KIT could be involved in the differentiation of thyroid cells and in tumor progression
low level of MITF (show MITF ELISA Kits) cooperates with oncogenic KIT to transform melanocytes. Activation of the cAMP pathway in transformed (L576P)KIT melanocytes stimulated MITF (show MITF ELISA Kits) expression, and reduced cellular proliferation and sphere formation. These findings highlight the essential role of MITF (show MITF ELISA Kits) in revealing the oncogenic activity of KIT in melanocytes and suggest that the cAMP pathway is a therapeutic target in KIT-mutated melanoma.
This previously unexplored G4-G4 interaction modulates both the conformation and the stability of the overall arrangement of the c-KIT promoter. It is not supported by stacking of single nucleotides but refers to a G4-G4 interaction surface surrounded by a two-nucleotides loop that might represent a reliable unprecedented target for anticancer therapy.
Transcription factor-induced activation of cardiac gene expression in human c-kit+ cardiac progenitor cells has been reported.
It was found that the absence of mutations in the SRSF2 (show SRSF2 ELISA Kits), ASXL1 (show ASXL1 ELISA Kits), and/or RUNX1gene panel at baseline and a reduction of the KIT D816V allele burden more than 25% at month 6 are the most favorable predictors for improved survival in midostaurin-treated advanced systemic mastocytosis patients.
Point mutation in c-kit gene is associated with sequential development of an ovarian mixed germ cell tumor and systemic mastocytosis with chronic myelomonocytic leukemia.
This study assesses MYB (show MYB ELISA Kits), CD117 and SOX-10 (show SOX10 ELISA Kits) expression in cutaneous adnexal tumors.
C-kit-positive hematopoietic stem/progenitor cells expressed significantly higher of Nox1 (show NOX1 ELISA Kits) and catalase (show CAT ELISA Kits), but less of lactoperoxidase (show LPO ELISA Kits) than in matured mononuclear cells.
c-KIT signaling regulates self-renewal capacity and prevents neurodifferentiation in culture.
These findings identify functional redundancy among Kit-dependent hematopoietic lineages and establish an unanticipated capacity of megakaryocytes to mediate IL-1 (show IL1A ELISA Kits)-driven systemic inflammatory disease.
WNT (show WNT2 ELISA Kits) signaling at an early stage (E12 (show ELSPBP1 ELISA Kits)-E15) of submandibular salivary gland (SMG (show SNRPG ELISA Kits)) development inhibits end bud morphogenesis and differentiation into proacini by suppressing Kit expression.
c-kit can reduce inflammation, positively modulate airway remodeling, and improve function in a mouse model of airway hyperresponsiveness
Kit inactivation within oocytes also led to premature ovarian failure, albeit via a contrasting phenotype. Despite normal initial complements of primordial follicles, oocytes remained dormant with arrested oocyte maturation. Foxo3 protein localization in the nucleus versus cytoplasm explained both mutant phenotypes.
sca-1 (show Ly6a ELISA Kits) antibody reduces both CD34 (show CD34 ELISA Kits)+/c-kit+ progenitor cell surge and vascular restenosis after endoluminal vascular injury in a murine model.
These findings indicate the SCF (show KITLG ELISA Kits)/Kit signaling insufficiency may contribute to the underdevelopment of ICCs and intestinal motility dysfunction upon hypoxia exposure.
we identified important roles for the GATA-2 C-ZnF in bone marrow hematopoiesis via control of c-Kit expression and HSC/HSPC survival.
IMC-G4 cells had an additional novel c-kit gene mutation of KIT-Tyr421Cys which is considered to induce neoplastic transformation of mouse mast cells
FGF7 (show FGF7 ELISA Kits) may be an important regulator for oocyte growth and its action is mediated via the KIT/KITLG (show KITLG ELISA Kits) signaling pathway.
mRNA expression of c-kit and SCF was decreased in gallbladder tissues in the HCD group. Consistent with the findings of RT-PCR, a lower expression level of c-kit and SCF protein was also observed in HCD animals.
Delayed enrichment for c-kit and inducing cardiac differentiation attenuated protective effects of BMSCs' transplantation in pig model of acute myocardial infarction.
Pravastatin improves function in hibernating myocardium by mobilizing CD133+ and cKit+ bone marrow progenitor cells and promoting myocytes to reenter the growth phase of the cardiac cell cycle.
c-kit is primarily expressed in the spermatogonia and spermatocytes of goat testes.
This gene encodes the human homolog of the proto-oncogene c-kit. C-kit was first identified as the cellular homolog of the feline sarcoma viral oncogene v-kit. This protein is a type 3 transmembrane receptor for MGF (mast cell growth factor, also known as stem cell factor). Mutations in this gene are associated with gastrointestinal stromal tumors, mast cell disease, acute myelogenous lukemia, and piebaldism. Multiple transcript variants encoding different isoforms have been found for this gene.
mast/stem cell growth factor receptor Kit
, p145 c-kit
, piebald trait protein
, proto-oncogene c-Kit
, proto-oncogene tyrosine-protein kinase Kit
, soluble KIT variant 1
, tyrosine-protein kinase Kit
, v-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene-like protein
, Dominant white spotting
, Steel Factor Receptor
, c-kit proto-oncogene protein
, dominant spotting
, spotted sterile male
, c-kit receptor tyrosine kinase
, mast/stem cell growth factor receptor
, protein kinase
, c-kit receptor
, mast cell growth factor receptor
, c-KIT gene1
, receptor tyrosine kinase c-kit
, Mast/stem cell growth factor receptor
, Proto-oncogene c-Kit
, Tyrosine-protein kinase Kit
, caprine c-kit protein