OXGR1 rabbit pAb

CAT:
855-ES11482-01
Size:
50 µL
  • Availability: 24/48H Stock Items & 2 to 6 Weeks non Stock Items.
  • Dry Ice Shipment: No
OXGR1 rabbit pAb - image 1

OXGR1 rabbit pAb

  • Background:

    This gene encodes a G protein-coupled receptor (GPCR) that belongs to the oxoglutarate receptor family within the GPCR superfamily. The encoded protein is activated by the citric acid intermediate, oxoglutarate, as well as several cysteinyl leukotrienes, including leukotrienes E4, C4 and D4, which are implicated in many inflammatory disorders. In mice, a knock-out of this gene leads to middle ear inflammation, changes in the mucosal epithelium, and an increase in fluid behind the eardrum, and is associated with hearing loss. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016]
  • Description:

    This gene encodes a G protein-coupled receptor (GPCR) that belongs to the oxoglutarate receptor family within the GPCR superfamily. The encoded protein is activated by the citric acid intermediate, oxoglutarate, as well as several cysteinyl leukotrienes, including leukotrienes E4, C4 and D4, which are implicated in many inflammatory disorders. In mice, a knock-out of this gene leads to middle ear inflammation, changes in the mucosal epithelium, and an increase in fluid behind the eardrum, and is associated with hearing loss. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2016],
  • UniProt:

    Q96P68
  • Swiss Prot:

    Q96P68
  • Reactivity:

    Human; Mouse; Rat
  • Immunogen:

    Synthesized peptide derived from human protein . at AA range: 130-210
  • Clonality:

    Polyclonal
  • Source:

    Rabbit
  • Applications:

    WB; ELISA
  • Concentration:

    1 mg/ml
  • Dilution:

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

    37kD
  • Storage Conditions:

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

    37kD
  • Fragment:

    IgG
  • Subcellular Location:

    Cell membrane; Multi-pass membrane protein.
  • Gene ID (Human):

    27199