HBS1L anticorps (AA 460-486)

N° du produit ABIN1538439

Cet anticorps anti-HBS1L est un anticorps Lapin Polyclonal détectant HBS1L dans WB. Adapté pour Humain et Souris.

Aperçu rapide pour HBS1L anticorps (AA 460-486) (ABIN1538439)

Antigène: HBS1L (HBS1-Like (HBS1L))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp HBS1L est non-conjugé

Application: Western Blotting (WB)

Clone: RB38809

Détail du produit anti-HBS1L anticorps

Épitope: AA 460-486

Homologie: B, Rat

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

Immunogène: 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.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:2000. WB: 1:2000. WB: 1:2000. WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

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

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

Date de péremption: 6 months

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.

Poids moléculaire: 75473

ID gène: 10767

NCBI Accession: NP_001138630, NP_001138679, NP_006611

UniProt: Q9Y450