FAM35A/B抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/10000. PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Belongs to the FAM35 family.,

FAM3D抗体应用：WB 1:500-2000, ELISA 1:10000-20000 similarity:Belongs to the FAM3 family.,tissue specificity:Abundantly expressed in placenta and weakly expressed in small intestine.,

FAM3D抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. similarity:Belongs to the FAM3 family.,tissue specificity:Abundantly expressed in placenta and weakly expressed in small intestine.,

FAM48A抗体应用：WB 1:500-2000, ELISA 1:10000-20000function:Required for MAP kinase p38 (MAPK11, MAPK12, MAPK13 and/or MAPK14) activation during gastrulation. Required for down-regulation of E-cadherin during gastrulation by regulating E-cadherin protein level downstream from NCK-interacting kinase (NIK) and independently of the regulation of transcription by Fgf signaling and Snail.,similarity:Belongs to the FAM48 family.,subunit:Interacts with MAPK14.,tissue specificity:Highly expressed in testis, moderately in brain and pituitary gland. Expressed in several fetal tissues, including lung, brain, thymus and kidney. Expression is down-regulated in malignant prostate tissues.,

FAM80A抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/20000. cofactor:Binds 2 manganese ions per subunit.,similarity:Belongs to the rimK family.,similarity:Contains 1 ATP-grasp domain.,

FAM80B抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/5000. cofactor:Binds 2 manganese ions per subunit.,similarity:Belongs to the rimK family.,similarity:Contains 1 ATP-grasp domain.,

FAN1抗体应用：WB 1:500-2000 This gene plays a role in DNA interstrand cross-link repair and encodes a protein with 5' flap endonuclease and 5'-3' exonuclease activity. Mutations in this gene cause karyomegalic interstitial nephritis. Alternatively spliced transcript variants encoding distinct isoforms have been described. [provided by RefSeq, Feb 2016],

FANCA抗体应用：Immunohistochemistry: 1/100 - 1/300. ELISA: 1/5000. Fanconi anemia complementation group A(FANCA) Homo sapiens The 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 breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group A. Alternative splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are the most common cause of Fanconi anemia. [provide

FANCB抗体应用：WB 1:500-2000 This gene encodes a member of the Fanconi anemia complementation group B. This protein is assembled into a nucleoprotein complex that is involved in the repair of DNA lesions. Mutations in this gene can cause chromosome instability and VACTERL syndrome with hydrocephalus. [provided by RefSeq, Apr 2016],

FANCD2抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Fanconi anemia complementation group D2(FANCD2) Homo sapiens The 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 breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group D2. This protein is monoubiquinated in response to DNA damage, resulting in its localization to nuclear foci with other proteins (BRCA