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LCA5 Antibody

Product Specifications

Background

LCA5 is a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternative splicing results in two transcript variants.

NCBI Gene ID

167691

Swiss Prot

Q86VQ0

Accession Number

NP_859065

Host

Rabbit

Reactivity

Human

Immunogen

Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human LCA5.

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Other

Purification

Antibody is purified by peptide affinity chromatography method.

Positive Control

Cat. No. 1211 - HepG2 Cell Lysate

Concentration

Batch dependent

Buffer

Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

For short periods of storage (days) store at 4˚ C. For longer periods of storage, store LCA5 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.

Calculated Molecular Weight

80 kDa

Applications Notes

LCA5 antibody can be used for detection of LCA5 by ELISA at 1:1562500. LCA5 antibody can be used for detection of LCA5 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Symbol

LCA5

NCBI Official Name

Leber congenital amaurosis 5

NCBI Organism

Homo sapiens

Background Reference 01

Ramprasad, V.L., (er) Mol. Vis. 14, 481-486 (2008) .

Other Product Names

LCA5, C6orf152

Tested Applications

ELISA, WB

Protein ID

170650670

Physical Properties

Liquid

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