ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining and in a rare syndrome

and in a rare syndrome known as alternating hemiplegia of childhood

cell adhesion and proliferation

stability and cross-linking by catalyzing post-translational 3-hydroxylation of proline residues

Available in a variety of colors to distinguish loops and needles of different specifications: white 1

NBEAL2 (neurobeachin-like protein 2)

ISPD Rabbit Polyclonal Antibody, 20ul Fluorescent Staining and in a rare syndromeThis gene encodes a 2 C methyl D erythritol 4 phosphate cytidylyltransferase like protein. Mutations in this gene are the cause of Walker Warburg syndrome. Alternate splicing results in multiple transcript variants.