RD3 Antibody
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.
NCBI Gene ID
343035
Swiss Prot
Q7Z3Z2
Host
Rabbit
Reactivity
Mouse, Rat
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 1-195 of human RD3 (NP_898882.1) .
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Neuroscience
Purification
Affinity purification
Positive Control
Mouse brain
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=14-830
Calculated Molecular Weight
Observed: 26kDa
Fragment
IgG
Applications Notes
WB: 1:500 - 1:1000
Symbol
RD3
Positive Control 2
Rat brain
NCBI Official Name
Retinal degeneration 3, GUCY2D regulator
NCBI Organism
Homo sapiens
Other Product Names
C1orf36, LCA12, protein RD3, retinal degeneration 3, retinal degeneration protein 3
Tested Applications
WB
Physical Properties
Liquid
Curated Selection
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