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Collagen
Host Mouse Application Immunohistochemistry on frozen sections (IHC-Fs),Immunohistochemistry (IHC) Reactivity Mouse Alternative names Mouse Type VII Collagen -
Collagen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),ELISA,Immunohistochemistry (IHC) Reactivity Mouse Alternative names Mouse Type VII Collagen (aa 757-967) NC1 FN-III-like Domains 7 and 8 -
Collagen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),ELISA,Immunohistochemistry (IHC) Reactivity Mouse Alternative names Mouse Type VII Collagen (aa 757-967) NC1 FN-III-like Domains 7 and 8 -
Laminin
Host Rabbit Reactivity Mouse Alternative names Mouse Laminin g 1 chain -
Laminin
Host Rabbit Reactivity Mouse Alternative names Mouse Laminin g 1 chain -
Nidogen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),ELISA,Western Blot (WB),Immunohistochemistry (IHC),Radioimmunoassay (RIA) Reactivity Mouse Alternative names Mouse Nidogen 1 -
Nidogen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),ELISA,Western Blot (WB),Immunohistochemistry (IHC),Radioimmunoassay (RIA) Reactivity Mouse Alternative names Mouse Nidogen 1 -
Nidogen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),Immunohistochemistry on paraffin sections (IHC-P),ELISA,Western Blot (WB),Immunohistochemistry (IHC),Radioimmunoassay (RIA) Reactivity Mouse Alternative names Mouse Nidogen 2 -
Nidogen
Host Rabbit Application Immunohistochemistry on frozen sections (IHC-Fs),Immunohistochemistry on paraffin sections (IHC-P),ELISA,Western Blot (WB),Immunohistochemistry (IHC),Radioimmunoassay (RIA) Reactivity Mouse Alternative names Mouse Nidogen 2 -
ABCB4/MDR3 Polyclonal
Description Mediates ATP-dependent export of organic anions and drugs from the cytoplasm. Hydrolyzes ATP with low efficiency. Human MDR3 is not capable of conferring drug resistance. Mediates the translocation of phosphatidylcholine across the canalicular membrane of the hepatocyte. Defects in ABCB4 are the cause of progressive familial intrahepatic cholestasis type 3 (PFIC3). PFIC3 is an autosomal recessive liver disorder presenting with early onset cholestasis that progresses to cirrhosis and liver failure before adulthood. It is characterized by elevated serum gamma-glutamyltransferase levels. Defects in ABCB4 are a cause of intrahepatic cholestasis of pregnancy (ICP); also known as obstetric cholestasis. ICP is a multifactorial liver disorder of pregnancy. It presents during the second or, more commonly, the third trimestre of pregnancy with intense pruritus which becomes more severe with advancing gestation and cholestasis. Cholestasis results from abnormal biliary transport from the liver in Host Rabbit Application ELISA, Immunohistochemistry (IHC), Western Blot (WB) Reactivity Human, Mouse