CYP4F22 antibody (Middle Region)
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- Target See all CYP4F22 Antibodies
- CYP4F22 (Cytochrome P450, Family 4, Subfamily F, Polypeptide 22 (CYP4F22))
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Binding Specificity
- Middle Region
- Reactivity
- Human, Cow, Dog, Horse, Pig, Rabbit, Mouse, Rat
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This CYP4F22 antibody is un-conjugated
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Application
- Western Blotting (WB)
- Sequence
- TLDSLQKCVF SYNSNCQEKM SDYISAIIEL SALSVRRQYR LHHYLDFIYY
- Predicted Reactivity
- Cow: 100%, Dog: 100%, Horse: 100%, Human: 100%, Mouse: 86%, Pig: 100%, Rabbit: 100%, Rat: 93%
- Characteristics
- This is a rabbit polyclonal antibody against CYP4F22. It was validated on Western Blot.
- Purification
- Affinity Purified
- Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of Human CYP4F22
- Top Product
- Discover our top product CYP4F22 Primary Antibody
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- Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
- Comment
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Antigen size: 531 AA
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- Lot specific
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Handling Advice
- Avoid repeated freeze-thaw cycles.
- Storage
- -20 °C
- Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Target
- CYP4F22 (Cytochrome P450, Family 4, Subfamily F, Polypeptide 22 (CYP4F22))
- Alternative Name
- CYP4F22 (CYP4F22 Products)
- Background
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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.
Alias Symbols: FLJ39501, LI3
Protein Interaction Partner: UBC,
Protein Size: 531 - Molecular Weight
- 62 kDa
- Gene ID
- 126410
- NCBI Accession
- NM_173483, NP_775754
- UniProt
- Q6NT55
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