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CYP4B1 Polyclonal Antibody

     
  • 1 - CYP4B1 Polyclonal Antibody AP69416
    Western Blot analysis of COLO cells using CYP4B1 Polyclonal Antibody
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P, IF, ICC, E
Primary Accession P13584
Reactivity Human, Rat, Mouse
Host Rabbit
Clonality Polyclonal
Calculated MW 58991 Da
Additional Information
Gene ID 1580
Other Names CYP4B1; Cytochrome P450 4B1; CYPIVB1; Cytochrome P450-HP
Dilution WB~~Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
IHC-P~~1:50~200
IF~~1:50~200
ICC~~N/A
E~~N/A
Format Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.09% (W/V) sodium azide.
Storage Conditions-20℃

For Research Use Only. Not For Use In Diagnostic Procedures.

Protein Information
Name CYP4B1 (HGNC:2644)
Function Catalyzes the omega- and (omega-1)-hydroxylation of saturated fatty acids and n-alkanes (By similarity). Also bioactivates xenobiotics such as the procarcinogen 3-methoxy-4-aminoazobenzene and the cyclic arylamines 2-aminofluorene and 2-aminoanthracene (By similarity). In addition, catalyzes O-dealkylation of 7-ethoxycoumarin (By similarity). Functions at the interface of xenobiotic and endobiotic metabolism, contributing both to fatty acid and hydrocarbon oxidation and to the bioactivation of diverse xenobiotics. Preferentially hydroxylates the terminal carbon (omega-hydroxylation) of medium-chain fatty acids (C8-C10), with regioselectivity decreasing as chain length increases. C8 fatty acids and C7 n-alkanes display optimal chain length for regioselective omega-hydroxylation, and n- alkanes (C7-C10) are generally turned over faster and with higher regioselectivity than the corresponding fatty acids. In addition to omega/omega-1 hydroxylation, also catalyzes alpha-, beta-, gamma- and delta-hydroxylation of mid-chain length fatty acids, whereas fatty alcohols of the same chain length are almost exclusively hydroxylated at the omega, omega-1 and omega-2 positions (By similarity).
Cellular Location Endoplasmic reticulum membrane {ECO:0000250|UniProtKB:P15128}; Peripheral membrane protein {ECO:0000250|UniProtKB:P15128}. Microsome membrane {ECO:0000250|UniProtKB:P15128}; Peripheral membrane protein {ECO:0000250|UniProtKB:P15128}
Tissue Location Detected in the liver and lung (at protein level).
Research Areas

BACKGROUND

Cytochromes P450 are a group of heme-thiolate monooxygenases. In liver microsomes, this enzyme is involved in an NADPH-dependent electron transport pathway. It oxidizes a variety of structurally unrelated compounds, including steroids, fatty acids, and xenobiotics.

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