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Rho-related GTP-binding protein antibody (C-Term)
RhO (pan)
Reactivity: Human
WB, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Rho-related GTP-binding protein Antibody
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Target
See all Rho-related GTP-binding protein (RhO (pan)) Antibodies
Rho-related GTP-binding protein (RhO (pan))
Binding Specificity
All epitopes for Rho-related GTP-binding protein antibodies
C-Term
Reactivity
All reactivities for Rho-related GTP-binding protein antibodies
Human
Host
All hosts for Rho-related GTP-binding protein antibodies
Rabbit
Clonality
All clonalities for Rho-related GTP-binding protein antibodies
Polyclonal
Conjugate
All conjugates for Rho-related GTP-binding protein antibodies
This Rho-related GTP-binding protein antibody is un-conjugated
Application
All applications for Rho-related GTP-binding protein antibodies
Western Blotting (WB), Immunohistochemistry (IHC)
Purpose
Rhodopsin Rabbit pAb
Sequence
NESFVIYMFV VHFTIPMIII FFCYGQLVFT VKEAAAQQQE SATTQKAEKE VTRMVIIMVI AFLICWVPYA SVAFYIFTHQ GSNFGPIFMT IPAFFAKSAA IYNPVIYIMM NKQFRNCMLT TICCGKNPLG DDEASATVSK TETSQVAPA
Cross-Reactivity
Mouse, Rat
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 200 to the C-terminus of human Rhodopsindopsin (NP_000530.1).
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000,IHC,1:50 - 1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for Rho-related GTP-binding protein
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Target
Rho-related GTP-binding protein (RhO (pan))
Alternative Name
RHO (RhO (pan) Products )
Background
Retinitis pigmentosa is an inherited progressive disease which is a major cause of blindness in western communities. It can be inherited as an autosomal dominant, autosomal recessive, or X-linked recessive disorder. In the autosomal dominant form,which comprises about 25 % of total cases, approximately 30 % of families have mutations in the gene encoding the rod photoreceptor-specific protein rhodopsin. This is the transmembrane protein which, when photoexcited, initiates the visual transduction cascade. Defects in this gene are also one of the causes of congenital stationary night blindness.,RHO,CSNBAD1,OPN2,RP4,rhodopsin,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),Neuroscience,RHO
Molecular Weight
38kDa
Gene ID
6010
UniProt
P08100
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