RPGR1 rabbit pAb

• Background :

  This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008]

• Description :

  This gene encodes a photoreceptor protein that interacts with retinitis pigmentosa GTPase regulator protein and is a key component of cone and rod photoreceptor cells. Mutations in this gene lead to autosomal recessive congenital blindness. [provided by RefSeq, Oct 2008],

• UniProt :

  Q96KN7

• Swiss Prot :

  Q96KN7

• Reactivity :

  Human; Mouse

• Immunogen :

  Synthesized peptide derived from human RPGR1 AA range: 256-306

• Target :

  RPGR1

• Clonality :

  Polyclonal

• Source :

  Rabbit

• Applications :

  WB

• Concentration :

  1 mg/ml

• Dilution :

  WB 1:500-2000

• Buffer :

  -20°C/1 year

• Storage Conditions :

  -20°C/1 year

• Fragment :

  IgG

• Subcellular Location :

  Cell projection, cilium . Situated between the axonemal microtubules and the plasma membrane (By similarity) . In the retinal photoreceptor cell layer, localizes at the connecting cilium, a thin bridge linking the cell body and the light-sensing outer segment (By similarity) . Colocalizes with RGPR in the photoreceptor connecting cilium (By similarity) . .

• Gene ID (Human) :

  57096