RD3 rabbit pAb
Product Specifications
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. [provided by RefSeq, Sep 2009]
Gene ID
343035
Swiss Prot
Q7Z3Z2
Cross Reactivity
Human; Mouse
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Dilution
WB 1: 500-2000
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage Conditions
-20°C/1 year
Available Sizes
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
MBS6383765-01 0.1 mL
KLRG1 (Killer Cell Lectin-like Receptor Subfamily G Member 1, 2F1-Ag, Mast Cell Function-associated Antigen 2F1, MAFA, MAFA-L, MGC123930) (FITC)
Sign In for Pricing
View Details MBS6383765-02 5x 0.1 mL
KLRG1 (Killer Cell Lectin-like Receptor Subfamily G Member 1, 2F1-Ag, Mast Cell Function-associated Antigen 2F1, MAFA, MAFA-L, MGC123930) (FITC)
Sign In for Pricing
View Details 128532-AP 100 µL
INPP5K (Inositol Polyphosphate 5-phosphatase K, Skeletal Muscle and Kidney-enriched Inositol Phosphatase, PPS, SKIP) (AP) discontinued
Sign In for Pricing
View Details 
ENZ-ABS614-0200 200 µg
β-Tubulin Recombinant monoclonal antibody (S11B) (Rabbit IgGλ)
Sign In for Pricing
View Details 