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Phospho-CaMKII (Thr286) Antibo

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月22日
  • W
  • Rabbit
  • H,M,R
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-CaMKII (Thr286) Antibody

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Thr286 of human CaMKII

    • 应用范围

      W

    • 宿主

      Rabbit

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H,M,R

    • 是否单克隆

      2

    • 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
    Reactivity Key:  H=Human  M=Mouse  R=Rat
    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) Source
    W H M R Endogenous 50 Rabbit
    Protocols
    Specificity / Sensitivity

    Phospho-CaMKII (Thr286) Antibody detects endogenous levels of CaMKII only when phosphorylated at Thr286.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr286 of human CaMKII. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Neuro2A cells treated with calcium ionophore (A23187, 2 µM) after a 20-minute preincubation with forskolin (30 μM), using Phospho-CaMKII (Thr286) Antibody (upper) or CaMKII Antibody #3362 (lower).

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Neuro2A cells, untreated or calf intestinal phosphatase (CIP)-treated, using Phospho-CaMKII (Thr286) Antibody (upper) or CaMKII Antibody #3362 (lower).

    Background

    CaMKII is an important member of the calcium/calmodulin-activated protein kinase family, functioning in neural synaptic stimulation and T-cell receptor signaling (1,2). CaMKII has catalytic and regulatory domains. The binding of Ca2+ /calmodulin to its regulatory domain releases its autoinhibitory effect and activates the kinase (3). The activated CaMKII further autophosphorylates at Thr286 to render the kinase constitutively active (3). The threonine phosphorylation state of CaMKII can be regulated through PP1/PKA. PP1 (protein phosphatase 1) dephosphorylates phospho-CaMKII at Thr286. PKA (protein kinase A) prevents this dephosphorylation through its inhibitory effect on PP1 (4).

    1. Hughes, K. et al. (2001) J. Biol. Chem. 276, 36008-36013.
    2. Barria, A. et al. (1997) Science 276, 2042-2045.
    3. Barkai, U. et al. (2000) Mol. Endocrinol. 14, 554-563.
    4. Makhinson, M. et al. (1999) J. Neurosci. 19, 2500-2510.
    5. Banno, Y. et al. (2008) J Neurochem 104, 1372-86.
    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
    • Ca2+/Calmodulin-Dependent Protein Kinase II (CaMKII)

      The Ca2+ /calmodulin (CaM)-dependent protein kinase II (CaMKII) is a major regulator of synaptic plasticity. CaMKII function depends on complex regulation of its activity and localization by Ca2+ /CaM and several auto-phosphorylation

    • Using Phospho‐Motif Antibodies to Determine Kinase Substrates

      comprising both the phosphorylated residue and the surrounding residues that determine kinase specificity, with degenerate residues taking up the remaining positions. Currently, several categories of phospho?motif antibody are commercially available

    • Optimized Protocol to Make Phospho-Specific Antibodies that Work

      , not simply its level of expression. In this review, we will discuss both the design of the phosphopeptide immunogen and immunization. The affinity purification of the phospho-specific antibody as well as the methods most suitable for characterizing

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