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PSMC3IP 抗体 (AA 1-100) (Cy7)

This anti-PSMC3IP antibody is a 兔 多克隆 antibody detecting PSMC3IP in IF (cc) 和 IF (p). Suitable for 小鼠.
产品编号 ABIN6986206
发货至: 中国

Quick Overview for PSMC3IP 抗体 (AA 1-100) (Cy7) (ABIN6986206)

抗原

See all PSMC3IP 抗体
PSMC3IP (PSMC3 Interacting Protein (PSMC3IP))

适用

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小鼠

宿主

  • 22
  • 1

克隆类型

  • 23
多克隆

标记

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This PSMC3IP antibody is conjugated to Cy7

应用范围

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Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • 抗原表位

    • 14
    • 4
    • 1
    • 1
    • 1
    AA 1-100

    交叉反应

    小鼠

    预测反应

    Human,Rat,Dog,Horse,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human PSMC3IP

    亚型

    IgG
  • 应用备注

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    有效期

    12 months
  • 抗原

    PSMC3IP (PSMC3 Interacting Protein (PSMC3IP))

    别名

    PSMC3IP

    背景

    Synonyms: 26S protease regulatory subunit 6A, 26S proteasome AAA-ATPase subunit RPT5, Human immunodeficiency virus tat transactivator binding protein 1, MGC8487, Proteasome (prosome macropain) 26S subunit ATPase 3, Proteasome 26S ATPase subunit 3, Proteasome 26S subunit ATPase 3, Proteasome subunit P50, PRS6A_HUMAN, PSMC 3, PSMC3, Tat binding protein 1, TAT-binding protein 1, TBP-1, TBP1.

    Background: This gene encodes a protein that functions in meiotic recombination. It is a subunit of the PSMC3IP/MND1 complex, which interacts with PSMC3/TBP1 to stimulate DMC1- and RAD51-mediated strand exchange during meiosis. The protein encoded by this gene can also co-activate ligand-driven transcription mediated by estrogen, androgen, glucocorticoid, progesterone, and thyroid nuclear receptors. Mutations in this gene cause XX female gonadal dysgenesis. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Dec 2011]

    基因ID

    29893

    UniProt

    Q9P2W1
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