HBa2 Protein (His tag)

Produktnummer ABIN1098667

Produktdetails

Target: HBa2 (Hemoglobin, alpha 2 (HBa2))

Protein-Typ: Recombinant

Spezies: Human

Quelle: Escherichia coli (E. coli)

Aufreinigungstag / Konjugat: Dieses HBa2 Protein ist gelabelt mit His tag.

Applikation: SDS-PAGE (SDS)

Reinheit: > 90 % by SDS - PAGE

Anwendungsinformationen

Kommentare:

Synonyms: Hemoglobin subunit alpha, nucleophosmin/nucleoplasmin 2

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/ml (determined by Bradford assay)

Buffer: 20 mM Tris-HCl buffer (pH 8.0) containing 0.1 M NaCl, 20% glycerol, 2 M Urea, 2 mM DTT

Lagerung: 4 °C

Informationen zur Lagerung: Avoid repeated freezing and thawing cycles.

Antigendetails

Target: HBa2 (Hemoglobin, alpha 2 (HBa2))

Andere Bezeichnung: HBA2 (HBa2 Produkte)

Synonyme: HBAM Protein, Hba-a1 Protein, Hba-a2 Protein, hba2 Protein, HBH Protein, hba5 Protein, HBA2 Protein, alpha globin Protein, HBA1 Protein, HBAI Protein, HBAII Protein, Glnc1 Protein, GloA Protein, hemoglobin, alpha 1 Protein, hemoglobin subunit alpha 1 S homeolog Protein, hemoglobin subunit alpha 2 Protein, hemoglobin subunit alpha 2 L homeolog Protein, hemoglobin subunit mu Protein, hemoglobin, alpha 2 Protein, hemoglobin subunit alpha-2-like Protein, hemoglobin alpha, adult chain 1 Protein, hemoglobin alpha, adult chain 2 Protein, Hba1 Protein, hba1.S Protein, HBA2 Protein, hba2.L Protein, HBM Protein, HBA Protein, Hba2 Protein, LOC102168959 Protein, Hba-a1 Protein, Hba-a2 Protein

Hintergrund: Hemoglobin subunit alpha, also known as HBA2, belongs to the globin family. HBA2 is involved in oxygen transport from the lung to the various peripheral tissues. The alpha-2(HBA2) and alpha-1 (HBA1) coding sequences are identical. These genes differ slightly over the 5' untranslated regions and the introns, but they differ significantly over the 3' untranslated regions. Two alpha chains plus two beta chains constitute HbA, which in normal adult life comprises about 97% of the total hemoglobin, alpha chains combine with delta chains to constitute HbA-2, which with HbF (fetal hemoglobin) makes up the remaining 3% of adult hemoglobin. Alpha thalassemias result from deletions of each of the alpha genes as well as deletions of both HBA2 and HBA1, some nondeletion alpha thalassemias have also been reported. Recombinant human HBA2 protein, fused to His-tag at N-terminus, was expressed in E.coli.

Molekulargewicht: 19.5 kDa (179aa)

NCBI Accession: NP_000508