Human CBL Antibody : APC (Phospho-Tyr774)

Katalog-Nummer OAAQ00187-100tests

Size : 100Tests

Marke : Aviva Systems Biology

Human CBL Antibody : APC (Phospho-Tyr774)

Human CBL Antibody : APC (Phospho-Tyr774) (OAAQ00187)

Datasheets/ManualsPrintable datasheet for OAAQ00187
Product Info
Tested Species ReactivityHuman, Mouse
Predicted Species ReactivityMouse, Rat
Product FormatLiquid. 1X PBS, 0.09% NaN3, 0.2% BSA.
ClonalityMonoclonal
CloneCblY774-R3B8
IsotypeRabbit IgG1k
HostRabbit
ConjugationAPC: Allophycocyanin
ApplicationFC
Reconstitution and Storage2-8C
ImmunogenA synthetic phospho-peptide corresponding to residues surrounding Tyr774 of human phospho c-Cbl
PurificationProtein A+G
Target Post-Translational ModificationPhospho-Tyr774
Application InfoFor flow cytometric staining, the suggested use of this reagent is 5 uL per million cells or 5 uL per 100 uL of staining volume. It is recommended that the reagent be titrated for optimal performance for each application.
Reference1. Christine, B.F. et al. (2001) Nat. Rev. Mol. Cell Biol. 2: 294-307.
2. Feshchenko, E.A. et al. (1998) J. Biol. Chem. 273: 8323-8331.
3. Blake, T.J. et al. (1991) Oncogene. 6: 653-657.
4. Thien, C.B. and Langdon, W.Y. (1998) Immunol. Cell Biol. 76: 473-482.
5. Kamei, T. et al. (2000) Int. J. Oncol. 17: 335-339.
Gene SymbolCBL
Gene Full NameCbl proto-oncogene
Alias SymbolsCBL2, NSLL, C-CBL, RNF55, FRA11B
NCBI Gene Id867
Protein NameE3 ubiquitin-protein ligase CBL
Description of TargetThis gene is a proto-oncogene that encodes a RING finger E3 ubiquitin ligase. The encoded protein is one of the enzymes required for targeting substrates for degradation by the proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder.
Uniprot IDP22681
Protein Accession #NP_005179.2
Nucleotide Accession #NM_005188.3