HBS1L Mouse Monoclonal Antibody [Kloon ID: LBI2A3]

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. [provided by RefSeq, May 2009]

Carrier-free (BSA/glycerol-free) HBS1L mouse monoclonal antibody, clone LBI2A3

EF-1a; eRF3c; ERFS; HBS1; HSPC276

Homo sapiens HBS1 like translational GTPase (HBS1L), transcript variant 1, mRNA.

10767

Q9Y450

Unconjugated

WB 1:500

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Lyophilized powder (original buffer 1X PBS, pH 7.3, 8% trehalose)

Stable for 1 year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. Aliquot will be stable at 4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

HBS1L

https://www.ncbi.nlm.nih.gov/gene/?term=10767

https://www.uniprot.org/uniprot/Q9Y450