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RhebL1 Antibody (C-14): sc-161185

 |  Datasheet

(Based on data analysis)

  • RhebL1 Antibody (C-14) is a goat polyclonal IgG provided at 200 µg/ml
  • epitope mapping near the C-terminus of RhebL1 of human origin
  • recommended for detection of RhebL1 of mouse, rat and human origin by WB, IP, IF and ELISA; also reactive with additional species, including equine, canine and bovine
  • blocking peptide, sc-161185 P
 

See additional Rheb Antibodies including Rheb and RhebL1.

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 Ordering Information
Product NameCatalog #UnitPriceQtyAdd 
RhebL1 Antibody (C-14) sc-161185 200 µg/ml $279
RhebL1 (C-14) P sc-161185 P
(peptide)
100 µg/0.5 ml $61
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human RHEBL1 121268 12q13.11 NM_144593 Q8TAI7
n/a
Mouse Rhebl1 69159 15 F1 NM_026967 Q9D8T3
N/A
 


RhebL1 (ras homolog enriched in brain-like protein 1), also known as Rheb2 or GTPase RhebL1, is a 183 amino acid protein that belongs to the small GTPase superfamily and Rheb family. Localizing to the cell membrane as well as the cytoplasm, RhebL1 is ubiquitously expressed and is increased two-fold in many tumor cell lines. RhebL1 exhibits GTPase activity and may activate NF-kappa-B-mediated gene transcription. Regulating the activity of Rictor, RhebL1 also promotes signal transduction. RhebL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 12q13.12 and mouse chromosome 15 F1. Human chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

RhebL1 Antibody (C-14) Data
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RhebL1 (C-14): sc-161185. Western blot analysis of RhebL1 expression in non-transfected: sc-117752 (A) and human RhebL1 transfected: sc-114548 (B) 293T whole cell lysates.
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