CP4FN rabbit pAb
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CP4FN rabbit pAb
Background :
Cytochrome P450 family 4 subfamily F member 22 (CYP4F22) Homo sapiens 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 gene is part of a cluster of cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12 (R) -lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3. [provided by RefSeq, Jul 2008]Description :
Cytochrome P450 family 4 subfamily F member 22 (CYP4F22) Homo sapiens 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 gene is part of a cluster of Cytochrome P450 genes on chromosome 19 and encodes an enzyme thought to play a role in the 12 (R)-lipoxygenase pathway. Mutations in this gene are the cause of ichthyosis lamellar type 3. [provided by RefSeq, Jul 2008],UniProt :
Q6NT55Swiss Prot :
Q6NT55Reactivity :
Human; Rat; MouseImmunogen :
Synthesized peptide derived from human protein . at AA range: 440-520Target :
CP4FNClonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
WB 1:500-2000 ELISA 1:5000-20000Buffer :
-20°C/1 yearMolecular Weight :
58kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
58kDFragment :
IgGSubcellular Location :
Endoplasmic reticulum membrane ; Single-pass type I membrane protein . Microsome membrane ; Single-pass type I membrane protein .Gene ID (Human) :
126410

