HBS1L Antikörper (AA 460-486)

Produktnummer ABIN7875126

Der Kaninchen Polyklonal anti-HBS1L Antikörper wird verwendet zum Nachweis von HBS1L in Proben von Human und Maus. Er wurde validiert für WB.

Kurzübersicht für HBS1L Antikörper (AA 460-486) (ABIN7875126)

Target: HBS1L (HBS1-Like (HBS1L))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HBS1L Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-HBS1L Antikörper

Bindungsspezifität: AA 460-486

Verwendungszweck: HBS1L Antibody

Aufreinigung: Antigen affinity purified

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

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: 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.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

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

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

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

Details zu HBS1L

Target: HBS1L (HBS1-Like (HBS1L))

Andere Bezeichnung: HBS1L

Hintergrund: 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