RP1L1 Antibodies

AND RP1L1 ELISA kits, RP1L1 Proteins

Many biological assays use antibodies to detect RP1L1, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with RP1L1 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop RP1L1 antibodies...

We validate the specificity of these antibodies to RP1L1 by testing them on tissues known to express RP1L1 positively and negatively. Browse below to find the RP1L1 antibody that suites your experiment. We have 0 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.

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RP1L1 Infographic by Boster Bio

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RP1L1 Overview

Facts about Retinitis pigmentosa 1-like 1 protein.

RP1L1 3D structure. Source: alphafold

Retinitis pigmentosa 1-like 1 protein (RP1L1)

Required for the differentiation of photoreceptor cells. Plays a role in the organization of outer segment of rod and cone photoreceptors (By similarity).

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Gene Information

Human
Gene Name:	RP1L1
Uniprot:	Q8IWN7
Entrez:	94137

Family

Belongs to:

No superfamily

Alternative Names

DCDC4B; Doublecortin Domain Containing 4B; Retinitis Pigmentosa 1 Like 1; Retinitis Pigmentosa 1-Like 1 Protein; Retinitis Pigmentosa 1-Like 1; RP1 Like 1

Molecular Weight

Mass (kDA):
252.289 kDA

Genomic Context


Human

Location:	8p23.1
Sequence:	8; NC_000008.11 (10606349..10655143, complement)

Tissue Specificity

Retinal-specific; expressed in photoreceptor.

Subcellular Localizations

Cytoplasm, cytoskeleton, cilium axoneme. Cell projection, cilium, photoreceptor outer segment. Localized to the axoneme of outer segments and connecting cilia in rod photoreceptors.

Diseases

Retinitis Pigmentosa
Dystrophy
Age Related Macular Degeneration
Retinal Diseases
Retinal Degeneration
Learning Disorders
Diabetic Retinopathy
Language Development Disorders
Chromosome Inversion
De Novo Mutation

Blind Vision
Epilepsy
Autistic Disorder
Speech Delay

Pathways

Phototransduction

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/RP1L1

References

PMID: 12724644 by Bowne S.J., et al. Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene.

PMID: 12634863 by Conte I., et al. Identification and characterization of the retinitis pigmentosa 1- like1 gene (rp1l1): a novel candidate for retinal degenerations.