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NSMCE2 抗体 (AA 151-250) (Cy7)

The 兔 多克隆 anti-NSMCE2 antibody is suitable to detect NSMCE2 in samples from 人. It has been validated for WB, IF (p) 和 IF (cc).
产品编号 ABIN896690
发货至: 中国
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Quick Overview for NSMCE2 抗体 (AA 151-250) (Cy7) (ABIN896690)

抗原

See all NSMCE2 抗体
NSMCE2 (E3 SUMO-Protein Ligase NSE2 (NSMCE2))

适用

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人

宿主

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兔

克隆类型

  • 65
  • 5
多克隆

标记

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This NSMCE2 antibody is conjugated to Cy7

应用范围

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

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    AA 151-250

    原理

    BCMP101 Polyclonal Antibody, Cy7 Conjugated

    预测反应

    Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Chicken,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human FAM84B/BCMP101

    亚型

    IgG
  • 应用备注

    WB(1:500-1000), 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, 0.02 % 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

    NSMCE2 (E3 SUMO-Protein Ligase NSE2 (NSMCE2))

    别名

    BCMP101

    背景

    Synonyms: BCMP101, Breast cancer membrane protein 101, Breast cancer membrane-associated protein 101, FA84B_HUMAN, FAM84B, Family with sequence similarity 84 member B, neurological/sensory 2, NSE2, OTTHUMP00000228215, Protein FAM84B, Protein NSE2, RGD1562236.

    Background: FAM84B, also known as NSE2 or BCMP101, is a 310 amino acid protein that is expressed in esophageal squamous cell carcinomas, suggesting a role in tumor development and metastasis. The gene encoding FAM84B maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

    基因ID

    157638
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