HBS1L antibody (AA 460-486)

Catalog No. ABIN1538439

This anti-HBS1L antibody is a Rabbit Polyclonal antibody detecting HBS1L in WB. Suitable for Human and Mouse.

Quick Overview for HBS1L antibody (AA 460-486) (ABIN1538439)

Target: HBS1L (HBS1-Like (HBS1L))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This HBS1L antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB38809

Product Details anti-HBS1L Antibody

Binding Specificity: AA 460-486

Predicted Reactivity: B, Rat

Purification: 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.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:2000. WB: 1:2000. WB: 1:2000. WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

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

Storage: 4 °C,-20 °C

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

Expiry Date: 6 months

Target Details for HBS1L

Target: HBS1L (HBS1-Like (HBS1L))

Alternative Name: HBS1L

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.

Molecular Weight: 75473

Gene ID: 10767

NCBI Accession: NP_001138630, NP_001138679, NP_006611

UniProt: Q9Y450