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FANCG(Phospho Ser383) Polyclonal Antibody, 20ul Pipette Holder probably as part of a

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FANCG(Phospho Ser383) Polyclonal Antibody, 20ul Pipette Holder probably as part of aThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal

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Description

probably as part of a linker structure which prevents centrosome splitting (PubMed: 18042621)

This O-methylation results in one of the major degradative pathways of the catecholamine transmitters

The receptor is a tetramer of different subunits (typically heterodimer of subunit 1 with one or more of subunits 2A-D)

HK3 encodes hexokinase 3

FANCG(Phospho Ser383) Polyclonal Antibody, 20ul Pipette Holder probably as part of aThe Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal

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