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Rabbit polyclonal to DLGAP2
ab106520 will not cross-react with other SAPAP proteins.
Mouse, Rat, Human
A 16 amino acid synthetic peptide from near the center of Human DLGAP2 (UniProt Q9P1A6).
WB: Raji and L1210 cell lysates;
ICC/IF: Human brain cells.
Shipped at 4°C. Store at 4°C (stable for up to 12 months).
Preservative: 0.02% Sodium Azide
Concentration information loading...
Immunogen affinity purified
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in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
Use a concentration of 20 µg/ml.
Use a concentration of 0.5 - 1 µg/ml. Predicted molecular weight: 118 kDa.
Use at an assay dependent concentration.
May play a role in the molecular organization of synapses and neuronal cell signaling. Could be an adapter protein linking ion channel to the subsynaptic cytoskeleton. May induce enrichment of PSD-95/SAP90 at the plasma membrane.
Expressed in brain and kidney.
Belongs to the SAPAP family.
Cell membrane. Cell junction > synapse > postsynaptic cell membrane > postsynaptic density. Cell junction > synapse. Postsynaptic density of neuronal cells.
Information by UniProt
Discs large (Drosophila) homolog associated protein 2 antibody
Western blot - Anti-DLGAP2 antibody (ab106520)
Lane 1 : Anti-DLGAP2 antibody (ab106520) at 0.5 µg/ml Lane 2 : Anti-DLGAP2 antibody (ab106520) at 1 µg/ml Lane 1 : Raji (human Burkitt's lymphoma cell line) cell lysate Lane 2 : Raji (human Burkitt's lymphoma cell line) cell lysate Predicted band size : 118 kDa
Western blot - DLGAP2 antibody (ab106520)
Lane 1 : Anti-DLGAP2 antibody (ab106520) at 0.5 µg/ml Lane 2 : Anti-DLGAP2 antibody (ab106520) at 1 µg/ml Lane 1 : L1210 cell lysate Lane 2 : L1210 cell lysate Lysates/proteins at 15 µg per lane. Predicted band size : 118 kDa
Immunocytochemistry/ Immunofluorescence-Anti-DLGAP2 antibody(ab106520)
Immunofluorescence of SAPAP2 in Human Brain cells using ab106520 at 20 ug/ml.
has not yet been referenced specifically in any publications.
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