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CAND1 (D1F2) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年12月18日
  • W, IP
  • H,M,R,Mk,C,Dg,Pg,GP
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      CAND1 (D1F2) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues surrounding Ala561 of human CAND1 protein

    • 应用范围

      W, IP

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 适应物种

      H,M,R,Mk,C,Dg,Pg,GP

    • 供应商

      CST

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting  IP=Immunoprecipitation
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey  C=Chicken  Dg=Dog  Pg=Pig  GP=Guinea Pig
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W IP H M R Mk (C) (Dg) (Pg) (GP) Endogenous 130 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    CAND1 (D1F2) Rabbit mAb recognizes endogenous levels of total CAND1 protein. Based upon sequence alignment, this antibody is not predicted to cross-react with CAND2/TIP120B.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Ala561 of human CAND1 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293T cells, either mock transfected (-) or transfected with a Myc-tagged cDNA expression construct encoding full-length human CAND1 (hCAND1-Myc, +), using CAND1 (D1F2) Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using CAND1 (D1F2) Rabbit mAb.

    Background

    Cullin-associated and neddylation-dissociated (CAND1)/TIP120A is a protein containing multiple HEAT repeats. It functions, in part, as an inhibitor of multiple cullin-RING ubiquitin ligases (CRLs) via binding to cullin-RBX complexes that are both unconjugated to NEDD8 and lack association with substrate recognition subunits (1-3). Indeed, CAND1 has been shown to bind all cullin family members in human cells and analysis of the crystal structure of human CAND1 bound to the CUL1-RBX1 complex suggests that CAND1 inhibits the activity of CRLs by sterically blocking both the substrate recognition subunit binding site and the NEDD8 conjugation site (1,3,4). Conversely, CAND1 binding to cullin-RBX complexes is incompatible with neddylation as NEDD8 conjugated to cullins blocks CAND1 binding, suggesting that CAND1 binds to cullins only after the COP9 signalosome has catalyzed cullin deneddylation. Through its ability to negatively regulate CRL assembly, CAND1 plays an integral part in facilitating CRL activation cycles that allow CRLs to utilize distinct substrate recognition subunits and protects these subunits from undergoing ubiquitin-dependent degradation (5-7).

    1. Liu, J. et al. (2002) Mol Cell 10, 1511-8.
    2. Zheng, J. et al. (2002) Mol Cell 10, 1519-26.
    3. Min, K.W. et al. (2003) J Biol Chem 278, 15905-10.
    4. Goldenberg, S.J. et al. (2004) Cell 119, 517-28.
    5. Wee, S. et al. (2005) Nat Cell Biol 7, 387-91.
    6. Wu, J.T. et al. (2005) Nat Cell Biol 7, 1014-20.
    7. Cope, G.A. and Deshaies, R.J. (2006) BMC Biochem 7, 1.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    图标文献和实验
    相关实验
    • Methods for the Detection of D-Amino-Acid Oxidase

      then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane was incubated

    • 组化染色背景高?没信号?一篇文章带你快速掌握免疫组化!

      组织化学分析。(图 C)使用Anti-Erk1/2 Mouse mAb 鼠单抗进行目的蛋白检测;(图 D) 使用p44/42 MAPK (Erk1/2)Rabbit mAb 兔单抗进行目的蛋白检测。 图 7 免疫组化实验检测Akt表达 注:使用 Anti-Akt (pan) Rabbit mAb 对正常小鼠肝组织进行免疫组织化学分析。(图 E)使用免疫组化试剂盒 M&R HRP/DAB Detection IHC Kit,抗体1:100 稀释;(图F)使用另一种试剂盒,抗体 1:100 稀释。

    • Methods for the Detection of D-Amino-Acid Oxidase

      min then twice for 5 min. It was incubated for 1 hr in TBS-T containing rabbit anti-hog D-amino-acid oxidase IgG (1/3,000 dilution) and quickly rinsed twice with TBS-T and further washed in TBS-T once for 15 min then twice for 5 min. The membrane

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