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    • monoclonal antibodies against cacybp sip  (Abcam)
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    Abcam monoclonal antibodies against cacybp sip
    The amino acid sequence of mouse <t>CacyBP/SIP</t> (accession number NP_033916). Lysine residues, identified by SUMOsp 2.0 tool, which might be potentially sumoylated are marked in bold (these with high probability) or underlined (these with lower probability)
    Monoclonal Antibodies Against Cacybp Sip, supplied by Abcam, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    The amino acid sequence of mouse CacyBP/SIP (accession number NP_033916). Lysine residues, identified by SUMOsp 2.0 tool, which might be potentially sumoylated are marked in bold (these with high probability) or underlined (these with lower probability)

    Journal: Neurochemical Research

    Article Title: The CacyBP/SIP Protein is Sumoylated in Neuroblastoma NB2a Cells

    doi: 10.1007/s11064-013-1155-4

    Figure Lengend Snippet: The amino acid sequence of mouse CacyBP/SIP (accession number NP_033916). Lysine residues, identified by SUMOsp 2.0 tool, which might be potentially sumoylated are marked in bold (these with high probability) or underlined (these with lower probability)

    Article Snippet: Proteins from the cell extract (80 μg) were analyzed by Western blot using monoclonal antibodies against CacyBP/SIP (Abcam).

    Techniques: Sequencing

    Co-immunoprecipitation of CacyBP/SIP with Ubc9 in NB2a cell extract. Cells were co-transfected with pGW1-HA-Ubc9 and pCMV3xFLAG-CacyBP/SIP (designated as HA-Ubc9 and 3xFLAG-CacyBP/SIP) or pGW1-HA-Ubc9 and pCMV3xFLAG (designated as HA-Ubc9). Proteins from the extract were used directly for Western blot analysis (80 μg) or incubated with anti-FLAG M2 affinity resin (800 μg). Proteins co-precipitated with CacyBP/SIP-3xFLAG were examined by Western blot using anti-Ubc9 or anti-CacyBP/SIP antibodies. Western blot images representative for 3 experiments performed are shown

    Journal: Neurochemical Research

    Article Title: The CacyBP/SIP Protein is Sumoylated in Neuroblastoma NB2a Cells

    doi: 10.1007/s11064-013-1155-4

    Figure Lengend Snippet: Co-immunoprecipitation of CacyBP/SIP with Ubc9 in NB2a cell extract. Cells were co-transfected with pGW1-HA-Ubc9 and pCMV3xFLAG-CacyBP/SIP (designated as HA-Ubc9 and 3xFLAG-CacyBP/SIP) or pGW1-HA-Ubc9 and pCMV3xFLAG (designated as HA-Ubc9). Proteins from the extract were used directly for Western blot analysis (80 μg) or incubated with anti-FLAG M2 affinity resin (800 μg). Proteins co-precipitated with CacyBP/SIP-3xFLAG were examined by Western blot using anti-Ubc9 or anti-CacyBP/SIP antibodies. Western blot images representative for 3 experiments performed are shown

    Article Snippet: Proteins from the cell extract (80 μg) were analyzed by Western blot using monoclonal antibodies against CacyBP/SIP (Abcam).

    Techniques: Immunoprecipitation, Transfection, Western Blot, Incubation

    Sumoylation of CacyBP/SIP in neuroblastoma NB2a cells. Western blot developed with anti-CacyBP/SIP antibody shows sumoylated CacyBP/SIP in cell extract ( A ) and in subcellular fractions of NB2a cells ( B ). In each case 80 μg of protein was applied on the gel. Panel C shows that wild type CacyBP/SIP (WT) is sumoylated in NB2a cell extract while K16R CacyBP/SIP mutant is not. Western blot images representative for 3 experiments performed are shown

    Journal: Neurochemical Research

    Article Title: The CacyBP/SIP Protein is Sumoylated in Neuroblastoma NB2a Cells

    doi: 10.1007/s11064-013-1155-4

    Figure Lengend Snippet: Sumoylation of CacyBP/SIP in neuroblastoma NB2a cells. Western blot developed with anti-CacyBP/SIP antibody shows sumoylated CacyBP/SIP in cell extract ( A ) and in subcellular fractions of NB2a cells ( B ). In each case 80 μg of protein was applied on the gel. Panel C shows that wild type CacyBP/SIP (WT) is sumoylated in NB2a cell extract while K16R CacyBP/SIP mutant is not. Western blot images representative for 3 experiments performed are shown

    Article Snippet: Proteins from the cell extract (80 μg) were analyzed by Western blot using monoclonal antibodies against CacyBP/SIP (Abcam).

    Techniques: Western Blot, Mutagenesis

    Model of the CacyBP/SIP N-terminal fragment (NTF) with bound SUMO1. The NTF structure of mouse CacyBP/SIP was taken from the Protein Data Bank (PDB; id:1YSM) as the first model of the 20 NMR structures . The structure of human SUMO1, which shares 100 % amino acid sequence identity with the mouse ortholog, was extracted from a crystal structure of the human SUMO E1 complex (PDB; id:3KYC) . Both proteins were bonded via residues K16 from NTF of CacyBP/SIP and G97 from the SUMO1 C-terminus. The K16 residue of CacyBP/SIP ( red ) and SUMO1 molecule are shown in semitransparent surfaces (Color figure online)

    Journal: Neurochemical Research

    Article Title: The CacyBP/SIP Protein is Sumoylated in Neuroblastoma NB2a Cells

    doi: 10.1007/s11064-013-1155-4

    Figure Lengend Snippet: Model of the CacyBP/SIP N-terminal fragment (NTF) with bound SUMO1. The NTF structure of mouse CacyBP/SIP was taken from the Protein Data Bank (PDB; id:1YSM) as the first model of the 20 NMR structures . The structure of human SUMO1, which shares 100 % amino acid sequence identity with the mouse ortholog, was extracted from a crystal structure of the human SUMO E1 complex (PDB; id:3KYC) . Both proteins were bonded via residues K16 from NTF of CacyBP/SIP and G97 from the SUMO1 C-terminus. The K16 residue of CacyBP/SIP ( red ) and SUMO1 molecule are shown in semitransparent surfaces (Color figure online)

    Article Snippet: Proteins from the cell extract (80 μg) were analyzed by Western blot using monoclonal antibodies against CacyBP/SIP (Abcam).

    Techniques: Sequencing