RAP1B rabbit pAb

CAT:
855-ES11183-01
Size:
50 µL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
RAP1B rabbit pAb - image 1

RAP1B rabbit pAb

  • Background:

    This gene encodes a member of the RAS-like small GTP-binding protein superfamily. Members of this family regulate multiple cellular processes including cell adhesion and growth and differentiation. This protein localizes to cellular membranes and has been shown to regulate integrin-mediated cell signaling. This protein also plays a role in regulating outside-in signaling in platelets. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 5, 6 and 9. [provided by RefSeq, Oct 2011]
  • Description:

    This gene encodes a member of the RAS-like small GTP-binding protein superfamily. Members of this family regulate multiple cellular processes including cell adhesion and growth and differentiation. This protein localizes to cellular membranes and has been shown to regulate integrin-mediated cell signaling. This protein also plays a role in regulating outside-in signaling in platelets. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 5, 6 and 9. [provided by RefSeq, Oct 2011],
  • UniProt:

    P61224
  • Swiss Prot:

    P61224
  • Reactivity:

    Human; Rat; Mouse
  • Immunogen:

    Synthesized peptide derived from human protein . at AA range: 110-190
  • Clonality:

    Polyclonal
  • Source:

    Rabbit
  • Applications:

    WB; ELISA
  • Concentration:

    1 mg/ml
  • Dilution:

    WB 1:500-2000 ELISA 1:5000-20000
  • Molecular Weight:

    20kD
  • Storage Conditions:

    -20°C/1 year
  • Observed Molecular Weight:

    20kD
  • Fragment:

    IgG
  • Subcellular Location:

    Cell membrane . Cytoplasm, cytosol . Cell junction . May shuttle between plasma membrane and cytosol (PubMed:3141412) . Presence of KRIT1 and CDH5 is required for its localization to the cell junction (PubMed:20332120) . .
  • Gene ID (Human):

    5908