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.

Classification:

Primary antibody

Alternative names:

RD3

Species reactivity:

Human, Mouse

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human RD3

Concentration:

1 mg/ml

Molecular weight:

21450

Applications:

WB

Storage:

-20°C for 1 year

More info:

Email: info@sobekbio.com

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