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ALK (31F12) Mouse mAb

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  • Cell Signaling Technology已认证
  • USA
  • 2025年12月26日
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    • 详细信息
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    • 技术资料
    • 抗体英文名

      ALK (31F12) Mouse mAb

    • 抗原

      recombinant protein containing a fragment near the carboxy terminus of human ALK

    • 应用范围

      W

    • 库存

      大量

    • 保质期

      详见说明书

    • 适应物种

      H

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 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
    Reactivity Key:  H=Human
    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 H Endogenous 220 (ALK), 80 (NPM-ALK) Mouse IgG1
    Protocols
    Specificity / Sensitivity

    ALK (31F12) Mouse mAb detects endogenous levels of total ALK protein. It does not cross-react with other related proteins.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a recombinant protein containing a fragment near the carboxy terminus of human ALK.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from Sup-M2 and KARPAS-299 cells using ALK (31F12) Mouse mAb.

    Background

    Anaplastic lymphoma kinase (ALK) is a tyrosine kinase receptor for pleiotrophin (PTN), a growth factor involved in embryonic brain development (1-3). In ALK-expressing cells, PTN induces phosphorylation of both ALK and the downstream effectors IRS-1, Shc, PLCγ, and PI3 kinase (1). ALK was originally discovered as a nucleophosmin (NPM)-ALK fusion protein produced by a translocation (4). Investigators have found that the NPM-ALK fusion protein is a constitutively active, oncogenic tyrosine kinase associated with anaplastic lymphoma (4). Research literature suggests that activation of PLCγ by NPM-ALK may be a crucial step for its mitogenic activity and involved in the pathogenesis of anaplastic lymphomas (5).A distinct ALK oncogenic fusion protein involving ALK and echinoderm microtubule-associated protein like 4 (EML4) has been described in the research literature from a non-small cell lung cancer (NSCLC) cell line, with corresponding fusion transcripts present in some cases of lung adenocarcinoma. The short, amino-terminal region of the microtubule-associated protein EML4 is fused to the kinase domain of ALK (6-8).

    1. Stoica, G.E. et al. (2001) J Biol Chem 276, 16772-9.
    2. Iwahara, T. et al. (1997) Oncogene 14, 439-49.
    3. Morris, S.W. et al. (1997) Oncogene 14, 2175-88.
    4. Morris, S.W. et al. (1994) Science 263, 1281-4.
    5. Bai, R.Y. et al. (1998) Mol Cell Biol 18, 6951-61.
    6. Rikova, K. et al. (2007) Cell 131, 1190-203.
    7. Takeuchi, K. et al. (2008) Clin Cancer Res 14, 6618-24.
    8. Soda, M. et al. (2007) Nature 448, 561-6.
    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
    • 【求助】关于ALK融合基因的检测

      肺癌病人的诊断和个性化治疗提供了有效的筛查工具。同样,以ROS1融合蛋白抗体(克隆号D4D6,货号#3287)为基础的IHC检测技术与断裂FISH方法相比,在非小细胞肺癌上IHC检测的准确度达到100%【5】。如此,我们期待检测ROS1融合变异的临床诊断用IHC试剂盒不久将成功推出。如要了解更多有关ALK和ROS1抗体的验证数据,请点击:ALK (D5F3) XP®Rabbit mAb #3633 和 ROS1 (D4D6) Rabbit mAb #3287。 本文

    • Purification of mAb (IgG)

      (adjust pH to 7.8 with Binding buffer; red color) to the Protein A column.Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10

    • Purification of mAb (IgG)

      ) to the Protein A column. Mouse antibodies of the IgG1 subclass do not have a high affinity for protein A. Purification on protein A beads using standard conditions will yield approximately 1/10 the amount of antibody compared with other subclasses

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