FKBP12 (FKBP1A) Mouse Monoclonal Antibody [Clone ID: OTI3B3]

CAT#: CF500557

Carrier-free (BSA/glycerol-free) FKBP1A mouse monoclonal antibody, clone OTI3B3 (formerly 3B3)

Specifications

Product Data

• Clone Name: OTI3B3
• Applications: FC, IHC, WB
• Recommended Dilution: WB: 1:200 - 1:1000, IHC 1:150, FLOW 1:100
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG2b
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human FKBP1A (NP_000792) produced in HEK293T cell.
• Formulation: Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)
• Reconstitution Method: For reconstitution, we recommend adding 100uL distilled water to a final antibody concentration of about 1 mg/mL. To use this carrier-free antibody for conjugation experiment, we strongly recommend performing another round of desalting process. (OriGene recommends Zeba Spin Desalting Columns, 7KMWCO from Thermo Scientific)
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Unconjugated
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 11.8 kDa
• Gene Name: Homo sapiens FKBP prolyl isomerase 1A (FKBP1A), transcript variant 1, mRNA.
• Database Link:
  NP_000792
  Entrez Gene 14225 MouseEntrez Gene 25639 RatEntrez Gene 2280 Human
  UniProt ID P62942
• Background: The protein encoded by this gene is a member of the immunophilin protein family, which play a role in immunoregulation and basic cellular processes involving protein folding and trafficking. The protein is a cis-trans prolyl isomerase that binds the immunosuppressants FK506 and rapamycin. It interacts with several intracellular signal transduction proteins including type I TGF-beta receptor. It also interacts with multiple intracellular calcium release channels, and coordinates multi-protein complex formation of the tetrameric skeletal muscle ryanodine receptor. In mouse, deletion of this homologous gene causes congenital heart disorder known as noncompaction of left ventricular myocardium. Multiple alternatively spliced variants, encoding the same protein, have been identified. The human genome contains five pseudogenes related to this gene, at least one of which is transcribed. [provided by RefSeq]
• Synonyms: FKBP-1A; FKBP-12; FKBP1; FKBP12; PKC12; PKCI2; PPIASE

Reference Data

• Protein Families: Druggable Genome