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Blood, Vol. 108, Issue 1, 362-369, July 1, 2006 This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef Identification of a homozygous deletion in the AP3B1 gene causing Hermansky-Pudlak syndrome, type 2 Blood Jung et al. 108: 362 Supplemental materials for: Jung et al Files in this Data Supplement: Table S1. Immunophenotypic analysis of peripheral blood lymphocytes of AP3-deficient patient (Patient #30) (PDF, 14.9 KB) Figure S1. Western Blot analysis of unfractionated protein extracts obtained from peripheral neutrophil granulocytes (JPG, 65.5 KB) - MPO – myeloperoxidase PR3 - proteinase-3 HNE - human neutrophil elastase MMP – matrix metalloproteinase 9 (gelatinase) Molecular markers are indicated. The membrane was stripped and reprobed to detect GAPDH confirming equal protein load. See “Materials/Methods” for details. This Article Abstract Full Text Services Email this article to a friend Alert me to new issues of the journal Rights and Permissions Citing Articles Citing Articles via CrossRef

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