|Tested Species reactivity||Human|
|Host / Isotype||Mouse / IgG1|
|Immunogen||RhoD human protein.|
|Contains||0.01% sodium azide|
|Storage conditions||4°C or -80°C if preferred|
MA1-7663 detects RhoD from human samples.
MA1-7663 has been successfully used in agglutination applications.
The MA1-7663 immunogen is RhoD human protein.
For short term storage, place at 4°C. For long term storage, place at -80°C.
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: ras homolog D; ras homolog gene family, member A; ras homolog gene family, member D; Rho-related GTP-binding protein RhoD; Rho-related protein HP1; RhoD; RhoHP1
Gene Aliases: ARHD; Rho; RHOD; RHOHP1; RHOM
UniProt ID: (Human) O00212
Entrez Gene ID: (Human) 29984
If an Invitrogen™ antibody doesn’t perform as described on our website or datasheet, we’ll replace the product at no cost to you, or provide you with a credit for a future purchase.*
Get expert recommendations for common problems or connect directly with an on staff expert for technical assistance related to applications, equipment and general product use.