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MITF encodes a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. Additionally we are shipping MITF Kits (11) and MITF Proteins (5) and many more products for this protein.
Showing 10 out of 130 products:
Human Polyclonal MITF Primary Antibody for ChIP, ICC - ABIN2452049
Osawa, Egawa, Mak, Moriyama, Freter, Yonetani, Beermann, Nishikawa: Molecular characterization of melanocyte stem cells in their niche. in Development (Cambridge, England) 2005
Show all 3 references for ABIN2452049
Human Monoclonal MITF Primary Antibody for ChIPSeq, ChIP - ABIN2668714
Du, Miller, Widlund, Horstmann, Ramaswamy, Fisher: MLANA/MART1 and SILV/PMEL17/GP100 are transcriptionally regulated by MITF in melanocytes and melanoma. in The American journal of pathology 2003
Show all 3 references for ABIN2668714
Human Monoclonal MITF Primary Antibody for EMSA, IHC (fro) - ABIN264430
Hägglund, Berghard, Carlsson: Canonical Wnt/?-catenin signalling is essential for optic cup formation. in PLoS ONE 2013
Show all 2 references for ABIN264430
Chicken Polyclonal MITF Primary Antibody for WB - ABIN2780334
Chiaverini, Beuret, Flori, Busca, Abbe, Bille, Bahadoran, Ortonne, Bertolotto, Ballotti: Microphthalmia-associated transcription factor regulates RAB27A gene expression and controls melanosome transport. in The Journal of biological chemistry 2008
Cow (Bovine) Polyclonal MITF Primary Antibody for WB - ABIN2777228
Schartl, Wilde, Laisney, Taniguchi, Takeda, Meierjohann: A mutated EGFR is sufficient to induce malignant melanoma with genetic background-dependent histopathologies. in The Journal of investigative dermatology 2009
Chicken Polyclonal MITF Primary Antibody for WB - ABIN2780333
Park, Wu, Yonemoto, Murphy-Smith, Wu, Stachur, Gilchrest: MITF mediates cAMP-induced protein kinase C-beta expression in human melanocytes. in The Biochemical journal 2006
Human Polyclonal MITF Primary Antibody for EIA, FACS - ABIN953453
Miller, Levy, Davis, Razin, Fisher: Sumoylation of MITF and its related family members TFE3 and TFEB. in The Journal of biological chemistry 2004
Accumulating mutations in series of haplotypes at the KIT and MITF loci are major determinants of white markings in Franches-Montagnes horses.
several independent mutations in MITF and PAX3 (show PAX3 Antibodies) together with known variants in the EDNRB (show EDNRB Antibodies) and KIT genes explain a large proportion of horses with the more extreme white spotting phenotypes.
Results show that Mitf, probably including Mitf-M, is expressed in the mitral cells and tufted cells that transmit the information derived from olfactory sensory neurons to the olfactory cortex.
SOX5 (show SOX5 Antibodies) has a strong inhibitory effect on MITF expression and seems to have a decisive clinical impact on melanoma during tumor progression.
In addition to melanoma risk, MITF p.E318K is associated with a high nevi count and could play a role in fast-growing melanomas.
expression of the molecular marker Mitf in primary cutaneous melanomas is a useful tool in assessing lymph node status.
an MITF-CEACAM1 (show CEACAM1 Antibodies) axis is suggested as a potential determinant of melanoma progression.
LEF-1 (show LEF1 Antibodies) and MITF regulate tyrosinase (show TYR Antibodies) gene transcription in vitro via binding to its promoter.
Here we show that MITF-A mRNA is predominantly expressed in all three human liver cancer cell lines examined.
Data show that mutant microphthalmia-associated transcription factor (MITF) with loss of localization signals (NLS (show ALDH1A2 Antibodies)) has failed to transactivate the transcriptional activities of target gene tyrosinase (TYR (show TYR Antibodies)), which can cause Waardenburg syndrome.
Data suggest that the heterozygous deletion mutation c.649_651delAGA in exon 7 of the microphthalmia-associated transcription factor (MITF) gene probably underlies the disease in the first family.
A reciprocal antagonism between the MITF and c-Jun (show JUN Antibodies) interconnects inflammation-induced dedifferentiation with pro-inflammatory cytokine responsiveness of melanoma cells favouring myeloid cell recruitment.
Therefore, it is reasonable to assume that the increase in the expression of Mitf in melanocytes is involved in the age-ssociated increase in the pigmentation in the eyes of black-eyed mice.
MITF interacts with BRG1 (show SMARCA4 Antibodies) to promote GATA4 (show GATA4 Antibodies) expression in cardiac hypertrophy.
Overexpression of FHL2 (show FHL2 Antibodies) alone had no effect on Erbin (show ERBB2IP Antibodies) expression, but in the presence of MITF, Erbin (show ERBB2IP Antibodies) expression was decreased.
BPTF (show BPTF Antibodies) likely acts as a cofactor for other transcription factors in MITF-negative melanoma cells and there are clearly genes regulated by BPTF (show BPTF Antibodies), but not MITF, in MITF-expressing lines.
the crucial role of signaling dependent MITF/p38 MAPK (show MAPK14 Antibodies) interactions in osteoclast differentiation
HDAC7 (show HDAC7 Antibodies) in osteoclasts is an important molecular regulator of MITF activity and bone homeostasis.
MITF-BRG1 (show SMARCA4 Antibodies) interplay thus plays an essential role in transcription regulation in melanoma.
Expression of microRNA-211 is regulated by the key melanocyte transcription factor MITF and regulates pigmentation by targeting the TGF-beta (show TGFB1 Antibodies) receptor 2.
Variability in the MITF gene clearly explained the differences between spotted and non-spotted cattle phenotypes but, at the same time, it is evident that this gene is not the only genetic factor determining piebaldism in two of the studied cattle breeds.
The objectives of this study were to characterize the phenotypes of German White Fleckvieh and to identify the mutation responsible for this newly detected phenotype in cattle using genome-wide association analyses and re-sequencing of MITF.
Although MITF does not seem to be the causal gene of the QTL initially observed, it can not be excluded that a prominent role of its transcription and function in the outbreak and evolution of the tumors observed in pigs.
This gene encodes a transcription factor that contains both basic helix-loop-helix and leucine zipper structural features. It regulates the differentiation and development of melanocytes retinal pigment epithelium and is also responsible for pigment cell-specific transcription of the melanogenesis enzyme genes. Heterozygous mutations in the this gene cause auditory-pigmentary syndromes, such as Waardenburg syndrome type 2 and Tietz syndrome. Alternatively spliced transcript variants encoding different isoforms have been identified.
microphthalmia transcription factor
, microphthalmia-associated transcription factor
, micophthalmia-associated transcription factor b
, class E basic helix-loop-helix protein 32
, black eyed white
, transcription factor
, microphtalmia-associated transcription factor