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  • Article number: A 1090.1
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    Vitamin D

    Host Rabbit
    Application ELISA
    Alternative names Vitamin D (Cholecalciferol)
    Unit 20 ul
    more info
    Normal leadtime 3 days
    Calculated total €89,00 
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  • Article number: A 1090.2
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    Vitamin D

    Host Rabbit
    Application ELISA
    Alternative names Vitamin D (Cholecalciferol)
    Unit 100 ul
    more info
    Normal leadtime 3 days
    Calculated total €440,00 
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  • Article number: A 1105.1
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    Zonulin

    Host Rabbit
    Application Immunohistochemistry on frozen sections (IHC-Fs),Immunohistochemistry on paraffin sections (IHC-P),ELISA,Immunohistochemistry (IHC)
    Reactivity Human
    Alternative names Human Zonulin (GGVLVQPG)
    Unit 20 ul
    more info
    Normal leadtime 3 days
    Calculated total €89,00 
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  • Article number: A 1105.2
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    Zonulin

    Host Rabbit
    Application Immunohistochemistry on frozen sections (IHC-Fs),Immunohistochemistry on paraffin sections (IHC-P),ELISA,Immunohistochemistry (IHC)
    Reactivity Human
    Alternative names Human Zonulin (GGVLVQPG)
    Unit 100 ul
    more info
    Normal leadtime 3 days
    Calculated total €440,00 
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  • Article number: RM0349
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    5T4 [EPR5529]

    Description 5T4 is a 72 kDa transmembrane glycoprotein that exhibits restricted expression in human and mouse adult tissues, is upregulated on many carcinomas and tumour expression correlates with poorer clinical outcome in ovarian, gastric and colorectal cancers. mES cells lack cell surface expression of the 5T4 antigen, and both protein and mRNA are rapidly upregulated following induction of differentiation. This proteins expression correlates with downregulation of OCT-4 and Tra-1–60. (Shipping Cost: €200.00)
    Host Rabbit
    Application Immunohistochemistry (IHC)
    Reactivity Human
    Unit 1 ml
    more info
    Normal leadtime 14 days
    Calculated total €494,00 
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  • Article number: MC0118
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    ABCB11/BRIC2/BSEP [MD122]

    Description Bile salt export pump (UniProt O95342; also known as ATP-binding cassette sub-family B member 11, Sister of P-glycoprotein) is encoded by the ABCB11 (also known as BRIC2, BSEP, PFIC2, SPGP) gene (Gene ID 8647) in human. Bile is produced by hepatocytes in the liver and released into the biliary system of ducts and gallbladder. After food ingestion, bile is released in the form of mixed micelles of salts and phospholipids into the duodenum where its detergent properties act to solubilize lipids to help their absorption by the intestine. Bile salt export pump is an ATP-binding cassette (ABC) family member localized to the hepatocyte canalicular membrane where it plays an important role in the bile salt-dependent bile flow and the normal enterohepatic circulation of bile salts from the distal intestine back to the liver. ABCB11/BSEP gene mutations are associated with progressive familial intrahepatic cholestasis type 2 (PFIC2), benign recurrent intrahepatic cholestasis type 2 (BRIC2), drug
    Host Mouse
    Application Immunohistochemistry (IHC), Western Blot (WB)
    Reactivity Human
    Unit 1 ml
    more info
    Normal leadtime 14 days
    Calculated total €401,70 
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  • Article number: MC0118RTU7
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    ABCB11/BRIC2/BSEP [MD122]

    Description Bile salt export pump (UniProt O95342; also known as ATP-binding cassette sub-family B member 11, Sister of P-glycoprotein) is encoded by the ABCB11 (also known as BRIC2, BSEP, PFIC2, SPGP) gene (Gene ID 8647) in human. Bile is produced by hepatocytes in the liver and released into the biliary system of ducts and gallbladder. After food ingestion, bile is released in the form of mixed micelles of salts and phospholipids into the duodenum where its detergent properties act to solubilize lipids to help their absorption by the intestine. Bile salt export pump is an ATP-binding cassette (ABC) family member localized to the hepatocyte canalicular membrane where it plays an important role in the bile salt-dependent bile flow and the normal enterohepatic circulation of bile salts from the distal intestine back to the liver. ABCB11/BSEP gene mutations are associated with progressive familial intrahepatic cholestasis type 2 (PFIC2), benign recurrent intrahepatic cholestasis type 2 (BRIC2), drug
    Host Mouse
    Application Immunohistochemistry (IHC), Western Blot (WB)
    Reactivity Human
    Unit 7 ml
    more info
    Normal leadtime 14 days
    Calculated total €187,20 
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  • Article number: RC0009
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    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
    Unit 1 ml
    more info
    Normal leadtime 14 days
    Calculated total €520,00 
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  • Article number: RC0009RTU7
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    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
    Unit 7 ml
    more info
    Normal leadtime 14 days
    Calculated total €254,80 
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  • Article number: MC0582
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    ABCG2/BCRP/CD338 [B1]

    Description Breast Cancer Resistance Protein (BCRP) is a 70 kDa ATP-Binding Cassette membrane transport protein involved in multidrug resistance. BCRP may be over-expressed in cancer cell lines selected with doxorubicin / verapamil, topotecan or mitoxantrone. Xenobiotic transporter that may play an important role in the exclusion of xenobiotics from the brain. May be involved in brain-to-blood efflux. Appears to play a major role in the multidrug resistance phenotype of several cancer cell lines. When overexpressed, the transfected cells become resistant to mitoxantrone, daunorubicin and doxorubicin, display diminished intracellular accumulation of daunorubicin, and manifest an ATP-dependent increase in the efflux of rhodamine 123. (Shipping Cost: €200.00)
    Host Mouse
    Application ELISA, Immunocytochemistry (ICC),Immunofluorescence (IF), Immunohistochemistry (IHC), Immunoprecipitation (IP), Western Blot (WB)
    Reactivity Human
    Unit 1 ml
    more info
    Normal leadtime 14 days
    Calculated total €361,40 
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