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PRPH2 antibody
PRPH2
Reactivity: Mouse, Rat
WB, IF, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-PRPH2 Antibody
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Target
See all PRPH2 Antibodies
PRPH2
(Peripherin 2 (Retinal Degeneration, Slow) (PRPH2))
Reactivity
All reactivities for PRPH2 antibodies
Mouse, Rat
Host
All hosts for PRPH2 antibodies
Rabbit
Clonality
All clonalities for PRPH2 antibodies
Polyclonal
Conjugate
All conjugates for PRPH2 antibodies
This PRPH2 antibody is un-conjugated
Application
All applications for PRPH2 antibodies
Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
Cross-Reactivity
Rat
Purification
Affinity purification
Immunogen
Recombinant protein corresponding to Mouse PRPH2/RDS
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Discover our top product PRPH2 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB (M,R) 1:1000-1:3000, IHC/IF (M,R) 1:2000-1:4000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS, pH 7.4, 0.02 % sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Target Details for PRPH2
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Target
PRPH2
(Peripherin 2 (Retinal Degeneration, Slow) (PRPH2))
Alternative Name
PRPH2/RDS (PRPH2 Products )
Synonyms
AOFMD antibody, AVMD antibody, Nmf193 antibody, PRPH antibody, RP7 antibody, Rd-2 antibody, Rd2 antibody, Rds antibody, Tspan22 antibody, rds antibody, RSRDS antibody, CACD2 antibody, DS antibody, RDS antibody, TSPAN22 antibody, rd2 antibody, CRDS1 antibody, prph-2 antibody, prph2b antibody, rds38 antibody, peripherin 2 antibody, peripherin 2 (retinal degeneration, slow) S homeolog antibody, Prph2 antibody, PRPH2 antibody, prph2.S antibody
Background
Peripherin-2 (PRPH2), also known as retinal degeneration slow protein (RDS), is a photoreceptor-specific tetraspanin protein implicated in outer segment disk morphogenesis. It may function as an adhesion molecule involved in stabilization and compaction of outer segment disks or in the maintenance of the curvature of the rim. Mutations in peripherin-2 are responsible for various retinal degenerative diseases including autosomal dominant retinitis pigmentosa (ADRP).
Molecular Weight
39 kDa
Gene ID
19133
UniProt
P15499
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