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SHIP1 (D1163) Antibody

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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年08月13日
  • W, IP
  • 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

      SHIP1 (D1163) Antibody

    • 抗原

      synthetic peptide corresponding to residues surrounding Asp1163 of human SHIP1

    • 应用范围

      W, IP

    • 宿主

      Rabbit

    • 供应商

      CST

    • 级别

      详见MSDS文件

    • 保质期

      详见说明书

    • 库存

      大量

    • 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  IP=Immunoprecipitation
    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 IP H M (R) Endogenous 145 Rabbit
    Protocols
    Specificity / Sensitivity

    SHIP1 (D1163) Antibody detects the endogenous levels of total SHIP1 protein.

    Source / Purification

    Polyclonal antibodies are produced by immunizing animals with a synthetic peptide corresponding to residues surrounding Asp1163 of human SHIP1. Antibodies are purified by protein A and peptide affinity chromatography.

    Western Blotting

    Western Blotting

    Western blot analysis of total cell lysates from RL, BaF3 and BW5147 cells, using SHIP1 (D1163) Antibody.

    Background

    SH2-containing inositol phosphatase 1 (SHIP1) is a hematopoietic phosphatase that hydrolyzes phosphatidylinositol-3,4,5-triphosphate to phosphatidylinositol-3,4-bisphosphate (1). SHIP1 is a cytosolic phosphatase with an SH2 domain in its amino terminus and two NPXY Shc binding motifs in its carboxy terminus (1,2). Upon receptor cross-linking, SHIP is first recruited to the membrane junction through binding of its SH2 domain to the phospho-tyrosine in the ITIM motif (2), followed by tyrosine phosphorylation on the NPXY motif (2). The membrane relocalization and phosphorylation on the NPXY motif is essential for the regulatory function of SHIP1 (3-5). Its effect on calcium flux, cell survival, growth, cell cycle arrest and apoptosis is mediated through the PI3K and Akt pathways (3-5). Tyr1021 is located in one of the NPXY motifs in SHIP1, and its phosphorylation is important for SHIP1 function (6).

    1. Tridandapani, S. et al. (1997) Mol Cell Biol 17, 4305-11.
    2. Liu, L. et al. (1997) J Biol Chem 272, 8983-8.
    3. Malbec, O. et al. (2001) J Biol Chem 276, 30381-91.
    4. Carver, D.J. et al. (2000) Blood 96, 1449-56.
    5. Scharenberg, A.M. et al. (1998) EMBO J 17, 1961-72.
    6. Sattler, M. et al. (2001) J Biol Chem 276, 2451-8.
    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
    • Analysis of Protein Complexes by 2D Blue Native/SDSPAGE and Antibody-Shift Assay

      Blue native polyacrylamide gel electrophoresis (BN-PAGE) is a powerful strategy for the separation of native multiprotein complex (MPC). Combined with other techniques, such as SDS–PAGE, immunoblotting, mass spectrometry, and antibody-shift

    • Antibody Conjugation

      has eluted into the column. c) Add 5mL of PBS on top. d)Open Stopcock. collect in 2mL fractions, discarding the first 2mL and keeping the 2nd 2mL fraction. The second 2mL fraction contains the conjugated antibody*. *NOTE: Step d) appropriate only if 1mL

    • Temperature-Dependent Antibody Kinetics as a Tool in Antibody Lead Selection

      Antibody–antigen interactions can principally be classified into three different temperature-dependent kinetic rate profiles. The affinity K D can persist, decrease, or increase in the temperature gradient. Today, the impact of temperature

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