
Supplier:
Aviva Systems Biology IncorporatedNCAM1 (neural cell adhesion molecule 1) Blocking Peptide (the C terminal of NCAM1)(100ug)
Prices direct from Aviva Systems Biology Incorporated
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SPECIFICATIONS
Size
100ug
Reactivities
Hum
Format
Lyophilized powder
Presku
AAP59939
Target
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.
Weight
39kDa
Gene Id
6010
Alternative Names
CSNBAD1; MGC138309; MGC138311; OPN2; RP4
Applications
FC
Hosts
Ham
Reactivities
Mouse
Applications
ELISA, WB
Hosts
Mouse
Applications
ELISA, IHC, WB
Hosts
Mouse
Applications
ELISA, FC
Hosts
Mouse
Reactivities
Bov
Applications
ELISA, IP, WB
Hosts
Mouse
Applications
ELISA, FC
Hosts
Mouse
Reactivities
Bov
Applications
FC
Hosts
Mouse
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