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FA2H polyclonal antibody

CAT: 0013-GTR18045865-02Size: 100 µLDry Ice: NoHazardous: No
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CAT#:0013-GTR18045865-02Size:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Rabbit polyclonal antibody to FA2H
Product Name Alternative
FA2H; FAAH; FAH1; FAXDC1; SCS7; SPG35
UniProt
Q7L5A8
Reactivity
Human, Rat
Immunogen
Recombinant fusion protein of human FA2H (NP_077282.3) .
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Metabolism Research
Purification
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE) .
Concentration
1mg/ml
Dilution
WB1:500 - 1:2000, IHC-P: -P1:50 - 1:200
Form
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2
Molecular Weight
38kDa
Storage Conditions
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Notes
For research use only.
Tested Applications
WB
Host or Source
Rabbit
Preservative
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH 7.2

UniProtKB · Q7L5A8

Fatty acid 2-hydroxylase

FA2H_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q7L5A8
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FA2H
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
1.14.18.-
Processing
—
Secondary accessions
B7Z8T6, O75213, Q96DK1, Q9H1A5
Protein keywords

Coding sequence diversity

Alternative splicing

Disease

Disease variantHereditary spastic paraplegiaLeukodystrophyNeurodegeneration

Cellular component

Endoplasmic reticulumMembraneMicrosome

Biological process

Fatty acid biosynthesisFatty acid metabolismLipid biosynthesisLipid metabolismSphingolipid metabolism

Ligand

HemeIronMetal-bindingZinc

Molecular function

Oxidoreductase

Technical term

Proteomics identificationReference proteome

Domain

TransmembraneTransmembrane helix

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