Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations [0]
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- Product number
- PAB10032 - Provider product page
- Provider
- Abnova Corporation
- Proper citation
- Abnova Corporation Cat#PAB10032, RRID:AB_1672186
- Product name
- CAND2 polyclonal antibody
- Antibody type
- Polyclonal
- Description
- Rabbit polyclonal antibody raised against synthetic peptide of CAND2.
- Storage
- Store at 4°C. For long term storage store at -20°C.Aliquot to avoid repeated freezing and thawing.
Submitted references Preferential interaction of TIP120A with Cul1 that is not modified by NEDD8 and not associated with Skp1.
CAND1 binds to unneddylated CUL1 and regulates the formation of SCF ubiquitin E3 ligase complex.
NEDD8 modification of CUL1 dissociates p120(CAND1), an inhibitor of CUL1-SKP1 binding and SCF ligases.
Multiple mammalian proteasomal ATPases, but not proteasome itself, are associated with TATA-binding protein and a novel transcriptional activator, TIP120.
Oshikawa K, Matsumoto M, Yada M, Kamura T, Hatakeyama S, Nakayama KI
Biochemical and biophysical research communications 2003 Apr 18;303(4):1209-16
Biochemical and biophysical research communications 2003 Apr 18;303(4):1209-16
CAND1 binds to unneddylated CUL1 and regulates the formation of SCF ubiquitin E3 ligase complex.
Zheng J, Yang X, Harrell JM, Ryzhikov S, Shim EH, Lykke-Andersen K, Wei N, Sun H, Kobayashi R, Zhang H
Molecular cell 2002 Dec;10(6):1519-26
Molecular cell 2002 Dec;10(6):1519-26
NEDD8 modification of CUL1 dissociates p120(CAND1), an inhibitor of CUL1-SKP1 binding and SCF ligases.
Liu J, Furukawa M, Matsumoto T, Xiong Y
Molecular cell 2002 Dec;10(6):1511-8
Molecular cell 2002 Dec;10(6):1511-8
Multiple mammalian proteasomal ATPases, but not proteasome itself, are associated with TATA-binding protein and a novel transcriptional activator, TIP120.
Makino Y, Yoshida T, Yogosawa S, Tanaka K, Muramatsu M, Tamura TA
Genes to cells : devoted to molecular & cellular mechanisms 1999 Sep;4(9):529-39
Genes to cells : devoted to molecular & cellular mechanisms 1999 Sep;4(9):529-39
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