RPGRIP1L Antibody / Protein fantom

• Description:

  The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5).

• UniProt:

  Q68CZ1

• Host:

  Rabbit

• Immunogen:

  E. coli-derived recombinant human protein (amino acids E608-D1264) was used as the immunogen for the RPGRIP1L antibody.

• Clonality:

  Polyclonal

• Isotype:

  IgG

• Applications:

  WB, FACS, Direct ELISA

• Format:

  Antigen affinity purified

• Buffer:

  0.5mg/ml if reconstituted with 0.2ml sterile DI water

• Reconstitution:

  After reconstitution, the RPGRIP1L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

• Limitations:

  This RPGRIP1L antibody is available for research use only.

• CAS Number:

  9007-83-4