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RAG1 (D36B3) Rabbit mAb

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2026年01月02日
  • W, IP
  • H
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      RAG1 (D36B3) Rabbit mAb

    • 抗原

      recombinant human RAG1 protein

    • 应用范围

      W, IP

    • 供应商

      CST

    • 库存

      大量

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 适应物种

      H

    • 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
    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 Endogenous 119 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    RAG1 (D36B3) Rabbit mAb detects endogenous levels of total RAG1 protein.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with recombinant human RAG1 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from MOLT-4 and HBP-ALL cells using RAG1 (D36B3) Rabbit mAb.

    Background

    The sequences encoding antigen receptors are split into multiple germline segments which are then combined by a process called V(D)J recombination during immune cells development. A variable (V) segment is combined with a joining (J) segment, and in some cases a D (Diversity) segment, to create the antigen-binding portion of the receptor. The recombined V(D)J segment is then spliced into exons that encode the constant region to produce mature mRNA (1,2). This essential process required for the development of functional immune T and B cells creates a vast diversity in these receptors (3,4). Initiation of this process follows binding of RAG1 (recombination activating gene 1) and RAG2 to the conserved recombination signal sequences (RSS) and the introduction of a double-strand break between the RSS and the coding sequence (5,6). RAG1 and RAG2 genes are located immediately adjacent to each other in the genome and lack introns in their coding regions in many species. RAG1 and RAG2 are coexpressed only in the B and T cell lineages and both are required for cleavage activity (7). RAG1 and RAG2 can also function as transposases, contributing to chromosomal translocations and lymphoid malignancy (8,9). Mutations in the RAG genes are associated with a spectrum of combined immune deficiencies in humans (10,11).

    1. Schatz, D.G. (2004) Semin Immunol 16, 245-56.
    2. Gellert, M. (2002) Annu Rev Biochem 71, 101-32.
    3. Alt, F.W. et al. (1992) Ann N Y Acad Sci 651, 277-94.
    4. Sadofsky, M.J. (2001) Nucleic Acids Res 29, 1399-409.
    5. Swanson, P.C. (2004) Immunol Rev 200, 90-114.
    6. Swanson, P.C. et al. (2009) Adv Exp Med Biol 650, 1-15.
    7. Fugmann, S.D. et al. (2000) Annu Rev Immunol 18, 495-527.
    8. Hiom, K. et al. (1998) Cell 94, 463-70.
    9. Agrawal, A. et al. (1998) Nature 394, 744-51.
    10. Villa, A. et al. (1999) J Clin Immunol 19, 87-97.
    11. Corneo, B. et al. (2000) J Biol Chem 275, 12672-5.
    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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