Lebercilin Antibodies

AND Lca5 ELISA kits, Lebercilin Proteins

Many biological assays use antibodies to detect Lebercilin, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Lebercilin in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Lebercilin antibodies...

We validate the specificity of these antibodies to Lebercilin by testing them on tissues known to express Lca5 positively and negatively. Browse below to find the Lca5 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

Previous: Septin9 Next: Cfap299

Lca5 Infographic by Boster Bio

All Lca5 Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-Lebercilin (LCA5) Mouse Monoclonal Antibody [Clone ID: OTI1A3]

Human

$523
Cat # M07874
100 µl

Lebercilin (LCA5) (NM_181714) Human Over-expression Lysate

Human

$628
Cat # LS167691
100 µg

Lca5 Overview

Facts about Lebercilin.

Lebercilin (Lca5)

Might be involved in minus end-directed microtubule transport. .

Gene Information

Mouse
Gene Name:	Lca5
Uniprot:	Q80ST9
Entrez:	75782

Family

Belongs to:

LCA5 family

Alternative Names

C6orf152Leber congenital amaurosis 5 protein; chromosome 6 open reading frame 152; Leber congenital amaurosis 5; Lebercilin

Molecular Weight

Mass (kDA):
80.162 kDA

Genomic Context


Mouse

Location:	9\|9 E2
Sequence:	9;

Tissue Specificity

Detected in several tissues.

Diseases

Amaurosis
Leber Congenital Amaurosis
Blind Vision
Dystrophy
Visual Impairment
Retinal Dystrophies
Retinal Degeneration
Retinitis Pigmentosa
Optic Atrophy, Hereditary, Leber
Retinal Diseases
Familial Aplasia Of The Vermis
Nystagmus

Atrophy
Congenital Ocular Coloboma (disorder)
Mutation, Out-of-frame
Macule
Respiration Disorders
Central Topographic Island

Pathways

Transport
Phototransduction
Phagocytosis
Cell Death
Pigmentation
Intraflagellar Transport
Protein Transport
Pathogenesis

Localization
Reflex

PTMs

Phosphoprotein

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Lca5

References

PMID: 17546029 by den Hollander A.I., et al. Mutations in LCA5, encoding the ciliary protein lebercilin, cause Leber congenital amaurosis.

PMID: 21606596 by Boldt K., et al. Disruption of intraflagellar protein transport in photoreceptor cilia causes Leber congenital amaurosis in humans and mice.