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CD55 Polyclonal Antibody, 50ul[BT-AP01735] Recombinant Protein Mutations in this gene have

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CD55 Polyclonal Antibody, 50ul[BT-AP01735] Recombinant Protein Mutations in this gene haveCCZ1, also known as CCZ1 vacuolar protein trafficking and biogenesis associated homolog (S. cerevisiae), CCZ1A, CCZ1B or CGI 43, is a 482 amino acid protein that localizes to the lysosomal membrane and belongs to the CCZ1 family. CCZ1 is encoded by a gene that maps to human chromosome 7, which houses over 1000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly,

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Description

Mutations in this gene have been associated with leukodystrophy dysmyelinating with spastic paraparesis with or without dystonia

a form of severe combined immunodef

SRSF8 encodes a member of a family of proteins containing a ribonucleoprotein (RNP)-type RNA binding motif and a carboxyl-terminal arginine-serine-rich (RS) domain

With a 75 mm membrane diameter

Belongs to the eukaryotic RPA43 RNA polymerase subunit family

CD55 Polyclonal Antibody, 50ul[BT-AP01735] Recombinant Protein Mutations in this gene haveCCZ1, also known as CCZ1 vacuolar protein trafficking and biogenesis associated homolog (S. cerevisiae), CCZ1A, CCZ1B or CGI 43, is a 482 amino acid protein that localizes to the lysosomal membrane and belongs to the CCZ1 family. CCZ1 is encoded by a gene that maps to human chromosome 7, which houses over 1000 genes and comprises nearly 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly,

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