1A36抗体应用：WB 1:500-2000

1B08抗体应用：WB 1:500-2000

1B81抗体应用：WB 1:500-2000

2B13抗体应用：WB 1:500-2000

2B17抗体应用：WB 1:500-2000

2B1G抗体应用：WB 1:500-2000

3pK抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.mitogen-activated protein kinase-activated protein kinase 3(MAPKAPK3) Homo sapiens This gene encodes a member of the Ser/Thr protein kinase family. This kinase functions as a mitogen-activated protein kinase (MAP kinase)- activated protein kinase. MAP kinases are also known as extracellular signal-regulated kinases (ERKs), act as an integration point for multiple biochemical signals. This kinase was shown to be activated by growth inducers and stress stimulation of cells. In vitro studies demonstrated that ERK, p38 MAP kinase and Jun N-terminal kinase were all able to phosphorylate and activate this kinase, which suggested the role of this kinase as an integrative element of signaling in both mitogen and stress responses. This kinase was reported to interact with, phosphorylate and repress the activity of E47, which is a bas

3β-HSD7抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7(HSD3B7) Homo sapiens This gene encodes an enzyme which is involved in the initial stages of the synthesis of bile acids from cholesterol and a member of the short-chain dehydrogenase/reductase superfamily. The encoded protein is a membrane-associated endoplasmic reticulum protein which is active against 7-alpha hydrosylated sterol substrates. Mutations in this gene are associated with a congenital bile acid synthesis defect which leads to neonatal cholestasis, a form of progressive liver disease. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2008],

4.1G抗体应用：Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Contains 1 FERM domain.,subunit:The CTD domain interacts with FKBP2 (By similarity). Interacts with FCGR1A.,tissue specificity:Widely expressed.,

4.1R 抗体应用：Western Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.erythrocyte membrane protein band 4.1(EPB41) Homo sapiens The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.[provided by RefSeq, Oct 2009],