RD3 Rabbit Polyclonal Antibody

Ab type

Primary antibody

Background

This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12| a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants.

Reactivity

Human, Mouse

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Immunogen

Synthesized peptide derived from human RD3

Storage Stability

-20°C for 1 year

Concentration

1 mg/ml

MolecularWeight_Da

21450

synonyms

RD3