BLM Antibody

BLM Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年10月17日
  • W
  • Rabbit
  • H
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    • 详细信息
    • 技术资料
    • 抗体英文名

      BLM Antibody

    • 抗原

      synthetic peptide corresponding to residues near the amino terminus of human BLM

    • 应用范围

      W

    • 宿主

      Rabbit

    • 供应商

      CST

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 适应物种

      H

    • 库存

      大量

    • 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
    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 Endogenous 190 Rabbit
    Protocols
    Specificity / Sensitivity

    BLM Antibody detects endogenous levels of total BLM protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues near the amino terminus of human BLM. Antibodies are purified by peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa and Jurkat cells using BLM Antibody.

    Background

    BLM, a member of the RecQ family of DNA helicases, is part of the BRCA1-associated genome surveillance complex (BASC) that responds to DNA damage, stalled replication forks and S phase arrest (1-4). Phosphorylation of BLM helicase at Thr99 and Thr122 occurs in response to genotoxic stress (4), and phosphorylation of Ser144 appears to be important in regulating chromosome stability during mitosis (5). Typical BLM protein resides in the nucleus and forms part of a dynamic protein complex that acts in response to DNA damage during specific periods of the cell cycle (6). Although RecQ helicases are rarely considered as essential enzymes, they function at the interface between DNA recombination and repair and are required for global genome stability maintenance. Mutations in BLM helicase are responsible for development of Bloom Syndrome, a recessive genetic disorder clinically characterized by short stature, immunodeficiency and elevated risk of malignancy (7). Similar alterations to genes encoding the related RecQ helicases RecQ4 and WRN also result in recessive genetic disorders associated with genomic instability (8,9). Cells from Bloom Syndrome patients exhibit genomic instability and increased frequency of sister chromatid exchange (10).

    1. Wang, Y. et al. (2000) Genes Dev. 14, 927-939.
    2. Langland, G. et al. (2002) Cancer Res. 62, 2766-2770.
    3. Sengupta, S. et al. (2003) EMBO J. 22, 1210-1222.
    4. Davies, S.L. et al. (2004) Mol. Cell. Biol. 24, 1279-1291.
    5. Leng, M. et al. (2006) Proc. Natl. Acad. Sci. USA 103, 11485-11490.
    6. Bischof, O. et al. (2001) J. Cell Biol. 153, 367-380.
    7. van Brabant, A.J. et al. (2000) Annu. Rev. Genomics Hum. Genet. 1, 409-459.
    8. Kitao, S. et al. (1999) Nat. Genet. 22, 82-84.
    9. Yu, C.E. et al. (1996) Science 272, 258-262.
    10. Chaganti, R.S. et al. (1974) Proc. Natl. Acad. Sci. USA 71, 4508-4512.
    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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