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HBS1L 抗体 (AA 293-622)

This 兔 多克隆 antibody specifically detects HBS1L in WB, ELISA 和 FACS. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7873454
发货至: 中国
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Quick Overview for HBS1L 抗体 (AA 293-622) (ABIN7873454)

抗原

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

适用

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人, 小鼠, 大鼠

宿主

  • 39
  • 7

克隆类型

  • 41
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多克隆

标记

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This HBS1L antibody is un-conjugated

应用范围

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Western Blotting (WB), ELISA, Flow Cytometry (FACS)
  • 抗原表位

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    AA 293-622

    原理

    HBS1L Antibody / HBS1-like protein

    纯化方法

    Immunogen affinity purified

    免疫原

    E.coli-derived human HBS1L recombinant protein (Position: H293-K622) was used as the immunogen for the HBS1L antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the HBS1L antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL

    缓冲液

    Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the HBS1L antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    HBS1L (HBS1-Like (HBS1L))

    别名

    HBS1L

    背景

    HBS1L antibody detects HBS1-like protein, encoded by the HBS1L gene on chromosome 6q23.3. HBS1L antibody is widely applied in studies of translation, mRNA surveillance, and hematopoiesis. HBS1L is a GTP-binding protein that functions in the no-go decay (NGD) pathway, a quality control mechanism that degrades mRNAs stalled during translation. It shares homology with translation elongation factors and interacts with the exosome complex and PELOTA to resolve stalled ribosomes. Expression is broadly detected across tissues, with particularly high levels in bone marrow and hematopoietic cells.

    Structurally, HBS1L is a ~70 kDa protein containing GTPase domains homologous to elongation factor 1a. These domains hydrolyze GTP to drive ribosome dissociation and recycling. A C-terminal domain mediates interactions with PELOTA and other decay machinery. Alternative splicing generates isoforms with distinct regulatory properties. Its domain organization reflects its role in linking translational control with RNA surveillance.

    Functionally, HBS1L participates in mRNA surveillance by recognizing stalled ribosomes and promoting their recycling. It collaborates with PELOTA to split ribosomes, freeing subunits for new rounds of translation. HBS1L also connects RNA quality control with hematopoietic differentiation, where it modulates globin gene expression and erythroid lineage decisions. Genome-wide association studies identify HBS1L variants as regulators of fetal hemoglobin levels. Researchers use HBS1L antibody to study mRNA decay, translation regulation, and blood cell development.

    Clinically, HBS1L is implicated in hematologic disorders and anemia. Genetic polymorphisms at the HBS1L-MYB intergenic region strongly influence fetal hemoglobin levels and modify disease severity in beta-thalassemia and sickle cell disease. These polymorphisms affect HBS1L expression and regulation, highlighting its clinical relevance. Dysregulated HBS1L expression also contributes to myelodysplastic syndromes and leukemias. NSJ Bioreagents supplies HBS1L antibody to support research in translation control, hematology, and RNA biology.

    Experimentally, HBS1L antibody is used in western blotting to detect the ~70 kDa protein, in immunohistochemistry to study bone marrow expression, and in immunofluorescence microscopy to examine cytoplasmic localization. Co-immunoprecipitation with HBS1L antibody identifies PELOTA and exosome complex partners involved in NGD.

    UniProt

    Q9Y450
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