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APC6 (D8D8) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月27日
  • W, IP
  • H,M,R,Mk,B,Dg,Pg
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      APC6 (D8D8) Rabbit mAb

    • 抗原

      synthetic peptide corresponding to residues near the carboxy terminus of human APC6 protein

    • 应用范围

      W, IP

    • 级别

      详见MSDS文件

    • 供应商

      CST

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H,M,R,Mk,B,Dg,Pg

    • 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  B=Bovine  Dg=Dog  Pg=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 (B) (Dg) (Pg) Endogenous 72 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    APC6 (D8D8) Rabbit mAb recognizes endogenous levels of total APC6 protein. Based upon sequence alignment, this antibody is not predicted to cross-react with either APC8/CDC23 or APC3/CDC27.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic peptide corresponding to residues near the carboxy terminus of human APC6 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from 293T cells, either mock transfected (-) or transfected with a Myc/DDK-tagged cDNA expression construct encoding full-length human APC6 (hAPC6-Myc/DDK, +), using APC6 (D8D8) Rabbit mAb.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from various cell lines using APC6 (D8D8) Rabbit mAb.

    Background

    Cell proliferation in all eukaryotic cells depends strictly upon the ubiquitin ligase (E3) activity of the anaphase promoting complex/cyclosome (APC/C), whose main function is to trigger the transition of the cell cycle from metaphase to anaphase. APC/C is a 1.5 MDa protein complex found in the nucleus of interphase cells. This complex diffuses throughout the cytoplasm and associates with parts of the spindle apparatus during mitosis. APC/C performs its various functions by promoting the assembly of polyubiquitin chains on substrate proteins, which targets these proteins for degradation by the 26S proteasome (1,2). In humans, twelve different APC/C subunits have been identified. Like all E3 enzymes, APC/C utilizes ubiquitin residues that have been activated by E1 enzymes and then transferred to E2 enzymes. Indeed APC/C has been shown to transiently interact with UBCH5 and UBCH10 E2 enzymes, in part, via the RING-finger domain-containing subunit, APC11 (3-5). In addition to E2 enzymes, APC/C activity is also strictly dependent upon one of several cofactors that associate with APC/C during specific phases of the cell cycle. The best studied of these are Cdc20 and Cdh1, which contain a C-terminal WD40 domain and participate in the recognition of APC/C substrates by interacting with specific recognition elements in these substrates (6), called D-Boxes (7) and KEN-boxes (8).

    APC6/CDC16 is a component of the tetratricopeptide repeat (TPR) sub-complex of the APC/C, which also consists of APC8/CDC23 and APC3/CDC27. It is thought that this sub-complex plays an important role in coordinating the juxtaposition of the catalytic and substrate recognition modules relative to co-activator, regulatory proteins, and substrates (9). There is also evidence suggesting that phosphorylation of APC6 and the other TPR subunits during mitosis plays a functional role in regulating the association between TPR subunits and substrate recognition subunits such as Cdc20 (10).

    1. Qiao, X. et al. (2010) Cell Cycle 9, 3904-12.
    2. Harper, J.W. et al. (2002) Genes Dev 16, 2179-206.
    3. Carroll, C.W. and Morgan, D.O. (2002) Nat Cell Biol 4, 880-7.
    4. Gmachl, M. et al. (2000) Proc Natl Acad Sci U S A 97, 8973-8.
    5. Leverson, J.D. et al. (2000) Mol Biol Cell 11, 2315-25.
    6. Kraft, C. et al. (2005) Mol Cell 18, 543-53.
    7. Glotzer, M. et al. (1991) Nature 349, 132-8.
    8. Pfleger, C.M. and Kirschner, M.W. (2000) Genes Dev 14, 655-65.
    9. Schreiber, A. et al. (2011) Nature 470, 227-32.
    10. Kraft, C. et al. (2003) EMBO J 22, 6598-609.
    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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