功能Rab effector protein involved in melanosome transport. Serves as link between melanosome-bound RAB27A and the motor protein MYO5A.
疾病相关Defects in MLPH are a cause of Griscelli syndrome type 3 (GS3) [MIM:609227]. GS3 is a rare autosomal recessive disorder characterized by pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts, and an accumulation of melanosomes in melanocytes, without other clinical manifestations.
Synaptotagmin like protein lacking C2 domains A antibody
Synaptotagmin-like protein 2a antibody
Anti-Melanophilin antibody 图像
Western blot - Melanophilin antibody (ab112954)
Anti-Melanophilin antibody (ab112954) at 1/100 dilution + A375 cell line lysate at 35 µg
Predicted band size : 66 kDa
Anti-Melanophilin antibody (ab112954)参考文献
This product has been referenced in:
Cetica V et al. Patients with Griscelli syndrome and normal pigmentation identify RAB27A mutations that selectively disrupt MUNC13-4 binding. J Allergy Clin Immunol135:1310-1318.e1 (2015).
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