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Rabbit anti-Human HBS1L Polyclonal Antibody

The antibody against HBS1L was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human HBS1L (NP_006611.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-01202A

The antibody against HBS1L was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human HBS1L (NP_006611.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-01202A ClonalityPolyclonal
Host SpeciesRabbitTarget NameHBS1L
Target SynonymsERFS; HBS1; EF-1a; eRF3c; HSPC276; HBS1LFormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.Purification MethodAffinity purification
Positive SamplesNIH/3T3, Mouse pancreasApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 1-260 of human HBS1L (NP_006611.1).Target SpeciesHuman
Uniprot IDQ9Y450Immunogen Sequence
Background Information
  • Uniprot Id

    Q9Y450

  • Target Species

    Human

  • Target Name

    HBS1L

  • Target Full Name

    HBS1-like protein

  • Target Function

    Cotranslational quality control factor involved in the No-Go Decay (NGD) pathway. In the presence of ABCE1 and PELO, is required for 48S complex formation from 80S ribosomes and dissociation of vacant 80S ribosomes. Together with PELO and in presence of ABCE1, recognizes stalled ribosomes and promotes dissociation of elongation complexes assembled on non-stop mRNAs; this triggers endonucleolytic cleavage of the mRNA, a mechanism to release non-functional ribosomes and to degrade damaged mRNAs as part of the No-Go Decay (NGD) pathway.; Facilitates the association of the exosome complex with the SKI complex.

  • Target Subcellular Location

    [Isoform 2]: Cytoplasm.

  • Target Protein Families

    TRAFAC class translation factor GTPase superfamily, Classic translation factor GTPase family

  • Target Tissue Specificity

    Detected in heart, brain, placenta, liver, muscle, kidney and pancreas.

  • Target Synonyms

    EF 1a; ERF3 similar protein; ERFS; HBS1; HBS1 like; HBS1 like protein; HBS1, S. cerevisiae, homolog of; HBS1-like (S. cerevisiae); HBS1-like protein; Hbs1l; HBS1L_HUMAN; Hsp70 subfamily B suppressor 1 like protein; HSPC276; KIAA1038

  • Target Background

    This gene encodes a member of the GTP-binding elongation factor family. It is expressed in multiple tissues with the highest expression in heart and skeletal muscle. The intergenic region of this gene and the MYB gene has been identified to be a quantitative trait locus (QTL) controlling fetal hemoglobin level, and this region influnces erythrocyte, platelet, and monocyte counts as well as erythrocyte volume and hemoglobin content. DNA polymorphisms at this region associate with fetal hemoglobin levels and pain crises in sickle cell disease. A single nucleotide polymorphism in exon 1 of this gene is significantly associated with severity in beta-thalassemia/Hemoglobin E. Multiple alternatively spliced transcript variants encoding different protein isoforms have been found for this gene.

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