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Western Blot at 1:1000 dilution Lane 1: human testis lysate Lane 2: Y79 whole cell lysate Lysates/proteins at 20 ug per lane.
Western blot analysis in 293 cell line lysates (35ug/lane).
Western Blot at 1:1000 dilution Lane 1: human testis lysate Lane 2: Y79 whole cell lysate Lysates/proteins at 20 ug per lane.

ELOVL4 Antibody

CATALOG NUMBER: 58-405

Clonality:
Polyclonal
Tested Applications:
WB
Host Species:
Rabbit
Species Reactivity:
Human
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human
Homology:
Predicted species reactivity based on immunogen sequence: Monkey
Immunogen:
This ELOVL4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 286-314 amino acids from the C-terminal region of human ELOVL4.
Conjugate:
Unconjugated
Tested Applications:
WB
Application Note:
For WB starting dilution is: 1:1000
Predicted Molecular Weight:
37 kDa
Purification:
This antibody is purified through a protein A column, followed by peptide affinity purification.
Clonality:
Polyclonal
Isotype:
Rabbit Ig
Physical State:
Liquid
Buffer:
Supplied in PBS with 0.09% (W/V) sodium azide.
Concentration:
batch dependent
Storage Conditions:
Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
Ncbi Official Symbol:
ELOVL4
Additional Names:
Elongation of very long chain fatty acids protein 4, 3-keto acyl-CoA synthase ELOVL4, ELOVL fatty acid elongase 4, ELOVL FA elongase 4, Very-long-chain 3-oxoacyl-CoA synthase 4, ELOVL4
Protein Accession Number:
Q9GZR5
Protein Gi Number:
20137966
Ncbi Gene Id Number:
6785
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
ELOVL4 is a membrane-bound protein which is amember of the ELO family, proteins which participate in thebiosynthesis of fatty acids. Consistent with the expression of theencoded protein in photoreceptor cells of the retina, mutations andsmall deletions in this gene are associated with Stargardt-likemacular dystrophy (STGD3) and autosomal dominant Stargardt-likemacular dystrophy (ADMD), also referred to as autosomal dominantatrophic macular degeneration.
Background Reference 1:
Kasperaviciute, D., et al. Brain 133 (PT 7), 2136-2147 (2010) :
Background Reference 2:
Vasireddy, V., et al. Prog Retin Eye Res 29(3):191-207(2010)
Background Reference 3:
Gu, H., et al. Zhonghua Yan Ke Za Zhi 46(2):125-128(2010)
Background Reference 4:
DeAngelis, M.M., et al. Arch. Ophthalmol. 125(1):49-54(2007)

FOR RESEARCH USE ONLY

For additional information, visit ProSci’s Terms & Conditions Page.

Disclaimer:
Optimal dilutions/concentrations should be determined by the end user. The information provided is a guideline for product use. This product is for research use only.

CATALOG NUMBER:

58-405

List Size:
400 ul

List Price:

$495.00

Datasheet
Shipping Info

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