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HBS1L 抗体 (AA 101-200) (AbBy Fluor® 488)

This anti-HBS1L antibody is a 兔 多克隆 antibody detecting HBS1L in WB, IF (cc) 和 IF (p). Suitable for 大鼠.
产品编号 ABIN1695681
发货至: 中国
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Quick Overview for HBS1L 抗体 (AA 101-200) (AbBy Fluor® 488) (ABIN1695681)

抗原

See all HBS1L 抗体
HBS1L (HBS1-Like (HBS1L))

适用

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大鼠

宿主

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克隆类型

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多克隆

标记

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This HBS1L antibody is conjugated to AbBy Fluor® 488

应用范围

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

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    AA 101-200

    交叉反应

    大鼠

    预测反应

    Human,Mouse,Dog,Pig,Rabbit

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human HBS1L

    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

    HBS1L (HBS1-Like (HBS1L))

    别名

    Hbs1l

    背景

    Synonyms: EF 1a, ERF3 similar protein, ERFS, HBS1, HBS1 like protein, HBS1L, Hsp70 subfamily B suppressor 1 like protein, KIAA1038, HBS1L_HUMAN.

    Background: HBS1L is a 684 amino acid protein that belongs to the GTP-binding elongation factor family and exists as multiple alternatively spliced isoforms. Expressed in kidney, brain, heart, placenta, liver, muscle and pancreas, HSB1L is thought to play a role in controlling fetal hemoglobin levels, specifically influencing platelet, monocyte and erythrocyte hemoglobin content. The gene encoding HBS1L maps to a locus on human chromosome 6 that is associated with sickle cell anemia and _-thalassemia, suggesting a role for HBS1L in the pathogenesis of blood disorders.

    基因ID

    10767
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