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ELOVL5 Rabbit Polyclonal Antibody

CAT: 0013-GTR17727853-01Size: 50 μLDry Ice: NoHazardous: No
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CAT#:0013-GTR17727853-01Size:50 μL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
ELOVL5 Rabbit Polyclonal Antibody
Product Name Alternative
ELOV5_HUMAN; ELOVL5; 3-keto acyl-CoA synthase ELOVL5; ELOVL fatty acid elongase 5 (ELOVL FA elongase 5) ; Elongation of very long chain fatty acids protein 5; Fatty acid elongase 1 (hELO1) ; Very long chain 3-ketoacyl-CoA synthase 5; Very long chain 3-oxoacyl-CoA synthase 5; 2.3.1.199; ELOVL2; ELOV5_MOUSE; ELOV5_RAT; Fatty acid elongase 1 (rELO1) ; ELOVL fatty acid elongase 5; ELOVL family member 5, elongation of long chain fatty acids (FEN1/Elo2, SUR4/Elo3-like, yeast) ; spinocerebellar ataxia 38
UniProt
Q9NYP7
Reactivity
Human, Rat
Immunogen
KLH conjugated synthetic peptide derived from human ELOVL5 (211-299/299aa)
Target
ELOVL5
Clonality
Polyclonal
Conjugation
Unconjugated
Field of Research
Metabolism Research
Purification
Affinity purified by Protein A
Concentration
1mg/ml
Dilution
WB=1:500-2000
Form
Liquid
Molecular Weight
33 kDa
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.
Prediction Reactivity
Canine, Mouse, Rabbit
Tested Applications
WB
Host or Source
Rabbit
Preservative
0.01M TBS (pH7.4) with 1% rAlbumin, 0.02% Proclin300 and 50% Glycerol.
Isotype
IgG

UniProtKB · Q9NYP7

Very long chain fatty acid elongase 5

ELOV5_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
Q9NYP7
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
ELOVL5
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.3.1.199
Processing
—
Secondary accessions
B4DZJ2, F6SH78, Q59EL3, Q5TGH5, Q6NXE7, Q7L2S5, Q8NCG4, Q9UI22
Protein keywords

PTM

AcetylationPhosphoprotein

Coding sequence diversity

Alternative splicing

Cellular component

Cell projectionEndoplasmic reticulumMembrane

Disease

Disease variantNeurodegenerationSpinocerebellar ataxia

Biological process

Fatty acid biosynthesisFatty acid metabolismLipid biosynthesisLipid metabolism

Technical term

Proteomics identificationReference proteome

Molecular function

Transferase

Domain

TransmembraneTransmembrane helix

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