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VRN2 抗体

This 小鼠 单克隆 antibody specifically detects VRN2 in ELISA 和 WB. It exhibits reactivity toward Triticum aestivum.
产品编号 ABIN7477853
发货至: 中国
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Quick Overview for VRN2 抗体 (ABIN7477853)

抗原

VRN2 (Polycomb Group Protein VERNALIZATION 2 (VRN2))

适用

Triticum aestivum

宿主

小鼠

克隆类型

单克隆

应用范围

ELISA, Western Blotting (WB)
  • 原理

    Anti-VRN2 | Vernalization protein 2

    交叉反应 (详细)

    Triticum aestivum
    Not reactive in: No confirmed exceptions from predicted reactivity are currently known

    预测反应

    Triticum monococcum

    纯化方法

    Protein G purified

    免疫原

    KLH-conjugated synthetic peptide chosen from Triticum aestivum VRN2 sequence
  • 应用备注

    1 : 10 000 (ELISA), 1 : 1000 (WB)

    说明

    there is some non-specific binding in a western blot when using anti-TaVRN2 antibody on nuclear extracts of T. monococcum

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    For reconstitution add 50 μL of sterile water

    缓冲液

    Total IgG. Protein G purified purified from Cell culture supernatant.

    注意事项

    Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube

    储存条件

    -20 °C

    储存方法

    Store lyophilized/reconstituted at -20°C, once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
  • 抗原

    VRN2 (Polycomb Group Protein VERNALIZATION 2 (VRN2))

    别名

    VRN2

    背景

    Background: Plants with a winter growth habit flower earlier when exposed for several weeks to cold temperatures, a process called vernalization. The wheat vernalization gene VRN-2 is a dominant repressor of flowering that is down-regulated by vernalization. Loss of function of VRN-2, whether by natural mutations or deletions, results in spring lines, which do not require vernalization to flower.

    Additional information: VRN-2 and ZCCT2 full-length proteins were expressed as GST fusion proteins in E. coli and purified through GST sepharose columns. The purified VRN-2 and ZCCT2 proteins were used to test the specificity of the VRN-2 antibody by Western blot analysis. A Western blot experiment showed that the VRN-2 antibody was able to differentiate VRN-2 from the ZCCT2 protein.

    分子量

    23.7 kDa
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