Welcome to Omnimabs!
TEL: 02154156726 Info: info@Omnimabs.com

Rabbit anti-CYP27A1 polyclonal antibody - middle region

Catalog Number:OM114508
OM114508
Discount Price
OM114508-100ul
1~2 Week
100ul
OM114508-50ul
50ul
OM114508-20ul
20ul
1~2 Week
Product Profile
Product Name Rabbit anti-CYP27A1 polyclonal antibody - middle region
Antibody Type Primary Antibodies
Antigen Alias CP27, CTX, CYP27
Immunogen The immunogen for anti-CYP27A1 antibody: synthetic peptide directed towards the middle region of human CYP27A1
Key Feature
Clonality Polyclonal
Isotype IgG
Host Species Rabbit
Tested Applications WB
WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Species Reactivity Human
Concentration 1mg/ml
Purification Affinity purified
Target Information
Gene Symbol CYP27A1
Gene Synonyms CP27
CTX
CYP27
Gene Full Name Cytochrome P450, family 27, subfamily A, polypeptide 1
Gene Summary CYP27A1 is 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. 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alternative Names CP27
CTX
CYP27
Molecular Weight(MW) 57kDa
Sequence 531 amino acids
Database Links
Entrez Gene 1593
SwissProt ID Q02318
Protein Accession NP_000775
Application

Western blot

0.2-1 ug/mlELISA Titer: 1:62500Positive Control: Human brain
Application Notes WB:1:500~1:2000
Notes:Optimal dilutions/concentrations should be determined by the researcher.
Additional Information
Form Liquid
Storage Instructions Aliquot and store at -20°C. Avoid repeated freeze / thaw cycles
Storage Buffer phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
validation
question title
question detaiil
Verification code