ELOVL Fatty Acid Elongase 4 (ELOVL4) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
ELOVL Fatty Acid Elongase 4 (ELOVL4) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx002627
tested applications
WB

Description

ELOVL4 Antibody is a Rabbit Polyclonal antibody against ELOVL4. This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
ELOVL Fatty Acid Elongase 4 (ELOVL4)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
60 µl
Size 2
120 µl
Size 3
200 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9GZR5
Gene ID
6785
NCBI Accession
NP_073563.1
Background
Antibody anti-ELOVL4
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

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ELOVL Fatty Acid Elongase 4 (ELOVL4) Antibody

ELOVL4 Antibody is a Rabbit Polyclonal antibody against ELOVL4. This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.

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