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The enzyme encoded by TYR catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. 再加上，我们可以发Tyrosinase 试剂盒 (58) 和 Tyrosinase 蛋白 (12)和数多这个蛋白质的别的产品。
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Fungus Polyclonal TYR Primary Antibody for ELISA, WB - ABIN2477015
Lezzi, Bleve, Spagnolo, Perrotta, Grieco: Production of recombinant Agaricus bisporus tyrosinase in Saccharomyces cerevisiae cells. in Journal of industrial microbiology & biotechnology 2012
Retinal pigment epithelium (which normally expresses tyrosinase) secretes a modulatory factor, possibly L-DOPA, which regulates light adaptation in the retinal circuitry.
Transcription of the tyrosinase gene family in an Atlantic salmon leukocyte cell line (SHK (显示 SHPK 抗体)-1) is influenced by temperature, but not by virus infection or bacterin stimulation.
Compound heterozygous mutations (c.832C>T and c.929_930insC) in the TYR gene may be responsible for partial clinical manifestations of oculocutaneous albinism
Mutations in tyrosinase gene is associated with Oculocutaneous albinism type 1.
tyrosinase as a potential GPR143 (显示 GPR143 抗体) binding protein opens new avenues for investigating the mechanisms that regulate pigmentation and neurogenesis.
Aberrant tyrosinase expression in an atypical fibroxanthoma
Findings suggested that miR (显示 MLXIP 抗体)-330-5p represents a potential tumor-suppressive miRNA and plays an important role in cutaneous malignant melanoma progression by suppressing TYR and PDIA3 (显示 PDIA3 抗体) expression.
Four missense substitutions (p.Arg239Trp, p.Ser192Tyr, p.Ser44Arg and p.Arg77Gln) were identified in tyrosinase in the families with oculocutaneous albinism linkage, and another missense substitution (p.Gln272Lys) was identified in the family with OCA4 linkage
LEF-1 (显示 LEF1 抗体) and MITF (显示 MITF 抗体) regulate tyrosinase gene transcription in vitro via binding to its promoter.
Data show that mutant microphthalmia-associated transcription factor (MITF (显示 MITF 抗体)) with loss of localization signals (NLS (显示 ALDH1A2 抗体)) has failed to transactivate the transcriptional activities of target gene tyrosinase (TYR), which can cause Waardenburg syndrome.
The tyrosinase gene was examined in 23 unrelated patients with autosomal recessive ocular albinism or nonsyndromic oculocutaneous albinism. TYR gene mutations were identi fi ed in 14 (app (显示 APP 抗体). 60%) albinism patients.
The two mutations (c.1114delG in the TYR gene and c.1426A>G in the OCA2 gene) may be responsible for partial clinical manifestations of Oculocutaneous albinism.
This study demonstrates the utility of CRISPR-Cas9 system in generating domain-specific in-frame deletions and helps gain further insights into structure-function of Tyr gene.
These results suggest that the tyrosinase-induced metabolism of rhodendrol causes melanocyte toxicity.
Data indicate that both ephedrannins A and B were competitive inhibitors of mushroom tyrosinase.
STAP-2 (显示 STAP2 抗体) colocalized with tyrosinase in lysosomes and protected tyrosinase from protein degradation in B16F10 melanoma cells.
Docosahexaenoic acid inhibits melanogenesis in B16F10 cells in vitro through increased tyrosinase degradation.
Studied upregulation by Kaliziri extract of tyrosinase, TRP-1 (显示 TRPC1 抗体), TRP-2 (显示 DCT 抗体) and MITF (显示 MITF 抗体) expression in murine B16 melanoma cells.
The albino mutation of tyrosinase alters ocular angiogenic responsiveness.
Tyrosinase is mutated in the albino dorsal lateral geniculate nucleus, arising from retinal ganglion cell misspecification together with potential perturbations of early activity patterns in the albino retina.
activated by ascorbic acid in B16 melanoma via p38 MAPK (显示 MAPK14 抗体) signaling and upregulation of melanogenic regulatory factors
Effect of zibuganshenfang on the expression and activity of tyrosinase on B16 cells
we identified some genes that are related to fur formation, including Tyrosinase-related protein 1 (TYRP1 (显示 TYRP1 抗体)) and Tyrosinase (TYR), as well as genes with unknown functions.
The enzyme encoded by this gene catalyzes the first 2 steps, and at least 1 subsequent step, in the conversion of tyrosine to melanin. The enzyme has both tyrosine hydroxylase and dopa oxidase catalytic activities, and requires copper for function. Mutations in this gene result in oculocutaneous albinism, and nonpathologic polymorphisms result in skin pigmentation variation. The human genome contains a pseudogene similar to the 3' half of this gene.
, hypothetical protein
, tyrosinase (oculocutaneous albinism IA)
, monophenol monooxygenase
, oculocutaneous albinism IA
, tumor rejection antigen AB
, albino locus protein