CYP27A1 Recombinant Protein (H00001593-P01)

CYP27A1 Recombinant Protein

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CYP27A1 Recombinant Protein Summary:
Species:Hu
Protein Type:Recombinant Protein
Applications:ELISA, WB
Gene:CYP27A1
Specificity:CYP27A1 (NP_000775.1, 1 a.a. - 531 a.a.) recombinant protein with a ~26kD N-terminal GST tag.
 
Note: Not all species have been tested for usefulness with this product. Only those species listed have been tested. We cannot make any guarantees about additional reactivities which may or may not occur.
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CYP27A1 Recombinant Protein Details:
Immunogen:This protein is not active and should not be used for experiments requiring activity.
Applications:
Uses:Western blot, ELISA. This protein has not been tested for any functionality. This product may contain endotoxins and is not suitable for use with live cells.
Dilutions:ELISA, Western Blot
Unit Size: 10 ug (also available: 25 ug)
Concentration:Please see the vial label for concentration.
Notes:
This product is produced by and distributed for Abnova, a company based in Taiwan.
Packaging:
Storage:Store at -80 °C. Avoid freeze-thaw cycles.
Buffer:50 mM Tris-HCI, 10 mM reduced Glutathione, pH=8.0 in the elution buffer.
Limitations:This product is for research use only and is not approved for use in humans or in clinical diagnosis. Products are guaranteed for 6 months from date of receipt, except for peptides and proteins which are guaranteed for 3 months.
Gene Symbol: CYP27A1
Entrez1593 (Human)
Swiss ProtNP_000775.1 (Human)
 
Background:

This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This mitochondrial protein oxidizes cholesterol intermediates as part of the bile synthesis pathway. Since the conversion of cholesterol to bile acids is the major route for removing cholesterol from the body, this protein is important for overall cholesterol homeostasis. Mutations in this gene cause cerebrotendinous xanthomatosis, a rare autosomal recessive lipid storage disease. [provided by RefSeq]

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