HBS1L anticorps (AA 293-622) (PE)

N° du produit ABIN7996085

Cet anticorps anti-HBS1L Polyclonal Lapin conjugué à PE (ABIN7996085) détecte spécifiquement HBS1L dans FACS. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour HBS1L anticorps (AA 293-622) (PE) (ABIN7996085)

Antigène: HBS1L (HBS1-Like (HBS1L))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBS1L est conjugé à/à la PE

Application: Flow Cytometry (FACS)

Détail du produit anti-HBS1L anticorps (PE)

Épitope: AA 293-622

Fonction: Anti-HBS1L Antibody PE Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Homologie: Human HBS1L shares 96.4%,97% amino acid (aa) sequence identity with mouse,rat HBS1L,respectively.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human HBS1L recombinant protein (Position: H293-K622). Human HBS1L shares 96.4% and 97% amino acid (aa) sequence identity with mouse and rat HBS1L, respectively.

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % 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: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur HBS1L

Antigène: HBS1L (HBS1-Like (HBS1L))

Autre désignation: HBS1L

Sujet:

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.

Gene Full Name: HBS1 like translational GTPase

ID gène: 10767

UniProt: Q9Y450