HBS1L anticorps (AA 460-486)

N° du produit ABIN7875126

L’anticorps anti-HBS1L Polyclonal Lapin est utilisé pour la détection de HBS1L dans des échantillons de Humain et Souris. Il a été validé pour WB.

Aperçu rapide pour HBS1L anticorps (AA 460-486) (ABIN7875126)

Antigène: HBS1L (HBS1-Like (HBS1L))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBS1L est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-HBS1L anticorps

Épitope: AA 460-486

Fonction: HBS1L Antibody

Purification: Antigen affinity purified

Immunogène: A portion of amino acids 460-486 from the human protein was used as the immunogen for the HBS1L antibody.

Isotype: Ig Fraction

Information d'application

Indications d'application: The stated application concentrations are suggested starting points. Titration of the HBS1L antibody may be required due to differences in protocols and secondary/substrate sensitivity.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: In 1X PBS, pH 7.4, with 0.09 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Aliquot the HBS1L antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur HBS1L

Antigène: HBS1L (HBS1-Like (HBS1L))

Autre désignation: HBS1L

Sujet: 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.

UniProt: Q9Y450