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NBPF5 Polyclonal Antibody, 20ul Immune Repertoire Sequencing Affected individuals display mottled pigmentation

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NBPF5 Polyclonal Antibody, 20ul Immune Repertoire Sequencing Affected individuals display mottled pigmentationNBPF5 (neuroblastoma breakpoint family member 5) is a 351 amino acid cytoplasmic protein that is expressed in medulla and brain and belongs to the NBPF family. NBPF5 contains one NBPF domain and is encoded by a gene that maps to human chromosome 1p13. Chromosome 1 spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease associated genes, including those that are

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Description

Affected individuals display mottled pigmentation

Altered copy number and activity of this gene have been observed in a number of human cancers

The protein encoded by CD99 is a cell surface glycoprotein involved in leukocyte migration

Tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins

exons 2 and 3 encode the alpha1 and alpha2 domains

NBPF5 Polyclonal Antibody, 20ul Immune Repertoire Sequencing Affected individuals display mottled pigmentationNBPF5 (neuroblastoma breakpoint family member 5) is a 351 amino acid cytoplasmic protein that is expressed in medulla and brain and belongs to the NBPF family. NBPF5 contains one NBPF domain and is encoded by a gene that maps to human chromosome 1p13. Chromosome 1 spans 260 million base pairs, contains over 3000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease associated genes, including those that are

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