HBS1L Antikörper (AA 460-486)

Produktnummer ABIN1538439

This anti-HBS1L antibody (ABIN1538439) is a Rabbit Polyclonal antibody detecting HBS1L in WB. Suitable for Human, Mouse.

Kurzübersicht für HBS1L Antikörper (AA 460-486) (ABIN1538439)

Target: HBS1L (HBS1-Like (HBS1L))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser HBS1L Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Klon: RB38809

Produktdetails anti-HBS1L Antikörper

Bindungsspezifität: AA 460-486

Homologie: B, Rat

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This HBS1L antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 460-486 amino acids from the Central region of human HBS1L.

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:2000. WB: 1:2000. WB: 1:2000. WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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: 4 °C,-20 °C

Informationen zur Lagerung: HBS1L Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

Details zu HBS1L

Target: HBS1L (HBS1-Like (HBS1L))

Andere Bezeichnung: HBS1L

Substanzklasse: Viral Protein

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.

Molekulargewicht: 75473

Gen-ID: 10767

NCBI Accession: NP_001138630, NP_001138679, NP_006611

UniProt: Q9Y450