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Involved in melanosome biogenesis by ensuring the stability of GPR143.
Showing 10 out of 728 products:
Human Monoclonal MLANA Primary Antibody for IHC (p) - ABIN535195
Zavala-Pompa, Folpe, Jimenez, Lim, Cohen, Eble, Amin et al.: Immunohistochemical study of microphthalmia transcription factor and tyrosinase in angiomyolipoma of the kidney, renal cell carcinoma, and renal and retroperitoneal sarcomas: comparative evaluation ... in The American journal of surgical pathology 2000
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Cow (Bovine) Monoclonal MLANA Primary Antibody for IHC (fro), IHC (p) - ABIN2475558
Chen, Stockert, Jungbluth, Tsang, Coplan, Scanlan, Old: Serological analysis of Melan-A(MART-1), a melanocyte-specific protein homogeneously expressed in human melanomas. in Proceedings of the National Academy of Sciences of the United States of America 1996
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Human Monoclonal MLANA Primary Antibody for ELISA, ICC - ABIN4333719
Joshi, Kooshki, Aldrich, Varghai, Zborowski, Singh, Triozzi: Expression of natural killer cell regulatory microRNA by uveal melanoma cancer stem cells. in Clinical & experimental metastasis 2016
Human Monoclonal MLANA Primary Antibody for IHC (p) - ABIN2475555
Moses: Muscle glycogenosis. in Journal of inherited metabolic disease 1990
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MART-1 (show RTL1 Antibodies) is a pigmentation gene that is required for melanosome biogenesis and/or maintenance.
Results suggest that the MART-1 (show RTL1 Antibodies)::Cre line may serve as a novel and useful tool for functional studies in melanocytes and retinal pigment epithelium.
OA1 (show GPR143 Antibodies) interacts with MART-1 (show RTL1 Antibodies) at early stages of melanogenesis to control melanosome identity and composition.
mLANA and p53 (show TP53 Antibodies) have roles in virus replication
Melan-A-stained slides shows definitive invasion.
Report automated quantification of proliferation with automated hot-spot selection in phosphohistone H3/MART1 dual-stained stage I/II melanoma.
Suggest MelanA-negative spindle-cell associated melanoma constitutes a distinct inflammatory phenotype correlated with dense infiltration of CD163 (show CD163 Antibodies) macrophages and loss of E-cadherin (show CDH1 Antibodies).
Inhibin alpha-subunit (show INHA Antibodies), Melan A and MNF116 were not sensitive for pheochromocytomas.
the presence of antibody and T-cell immune responses directed against the melanocyte-differentiation-antigens MART-1 (Melan-A), tyrosinase (show TYR Antibodies) and gp100 (show PMEL Antibodies) in patients with melanoma-associated (show ZNF654 Antibodies) leucoderma, as compared to patients with vitiligo (show MITF Antibodies).
Knockdown of T-bet expression in Mart (show SEPT4 Antibodies)-127-35 -specific T-cell-receptor-engineered human CD4 (show CD4 Antibodies)(+) CD25 (show IL2RA Antibodies)(-) and CD8 (show CD8A Antibodies)(+) T cells attenuates effector function.
Melan-A was useful to confirm the diagnosis of lentigo maligna in early lesions and to differentiate these from chronically sun-damaged skin.
Misinitiation of intrathymic MART-1 transcription and biased TCR usage explain the high frequency of MART-1-specific T cells.
Comprehensive characterization of the marginal and joint distributions for S100, HMB-45, and Melan-A across a large series of cutaneous melanomas revealed diversity of expression across this group of antigens.
melan A (A103) is not expressed in mesotheliomas
Involved in melanosome biogenesis by ensuring the stability of GPR143. Plays a vital role in the expression, stability, trafficking, and processing of melanocyte protein PMEL, which is critical to the formation of stage II melanosomes.
melanoma antigen recognized by T-cells 1
, melanoma associated antigen recognized by T-cells 1
, antigen LB39-AA
, antigen SK29-AA
, protein Melan-A