Hemoglobin, alpha 2 Proteine (HBa2)

The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. Zusätzlich bieten wir Ihnen HBa2 Antikörper (15) und viele weitere Produktgruppen zu diesem Protein an.

alle Proteine anzeigen Gen GeneID UniProt
Ratte HBa2 HBa2 360504 P01946
HBa2 3040 P69905
HBa2 379435 P06638
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Showing 6 out of 6 products:

Katalog Nr. Origin Quelle Konjugat Bilder Menge Anbieter Lieferzeit Preis Details
HOST_Escherichia coli (E. coli) Human His tag 100 μg Anmelden zum Anzeigen 11 bis 15 Tage
303,81 €
HOST_Wheat germ Human GST tag 10 μg Anmelden zum Anzeigen 7 bis 8 Tage
345,60 €
Hefe Xenopus laevis His tag   1 mg Anmelden zum Anzeigen 58 bis 70 Tage
2.193,02 €
HOST_Escherichia coli (E. coli) Human His tag   100 μg Anmelden zum Anzeigen 7 bis 8 Tage
358,40 €
HOST_Escherichia coli (E. coli) Human Unkonjugiert   100 μg Anmelden zum Anzeigen 6 bis 8 Tage
374,15 €
Hefe Human Unkonjugiert   100 μg Anmelden zum Anzeigen 7 bis 12 Tage
307,74 €

HBa2 Proteine nach Spezies und Herkunft

Origin Exprimiert in Konjugat
Human , ,
Xenopus laevis

Am meisten referenzierte HBa2 Proteine

  1. Human HBa2 Protein expressed in Escherichia coli (E. coli) - ABIN1098667 : Abdulmalik, Safo, Lerner, Ochotorena, Daikhin, Lakka, Santacroce, Abraham, Asakura: Characterization of hemoglobin bassett (alpha94Asp-->Ala), a variant with very low oxygen affinity. in American journal of hematology 2004 (PubMed)
    Zeige alle 2 Referenzen für 1098667

Weitere Proteine zu Hemoglobin, alpha 2 (HBa2) Interaktionspartnern

Horse (Equine) Hemoglobin, alpha 2 (HBa2) Interaktionspartner

Human Hemoglobin, alpha 2 (HBa2) Interaktionspartner

  1. Carriers of Hb Nanning are asymptomatic and could be missed by screening based on MCV and MCH (zeige PMCH Proteine) cutoffs of <80.0 fL and <27.0 pg, respectively. Both carriers of the mutation in the study have MCV and MCH (zeige PMCH Proteine) values that are 2 standard deviations (SDs (zeige SDS Proteine)) below normal, as would be predicted for an alpha+-thal.

  2. Data indicate that binding of hemoblobin (Hb) to glycoprotein1balpha (GP1balpha) induced platelet activation plays a crucial role in thrombus formation on immobilized von Willebrand factor (VWF (zeige VWF Proteine)) or type I collagen under shear stresses.

  3. Hb Adana mutation was preferentially present in the alpha2-globin genes in Malays compared to the other ethnicities in Malaysia.

  4. Seven novel nondeletional alpha-thalassemia mutations localized on the alpha2-globin gene in the heterozygous state were identified

  5. Gene frequency for HBA2:c.301-24delGinsCTCGGCCC carriers among the Chinese population in Guangxi.

  6. Hemoglobin Constant Spring mutation in Southeast Asians with thalassemia.

  7. We report herein for the first time the description of HbA2' in the Tunisian population.

  8. In maturing RBC (zeige CACNA1C Proteine) progenitors AHSP (zeige aHSP Proteine) bind to free alpha-globin (zeige HBA1 Proteine) chains to increase the HbA (zeige SCN2A Proteine) production. (Review)

  9. Two mutations detected the -a(3,7) single gene deletion found in 75% of cases and the nongene deletion a2 IVS1 [-5nt (zeige ACPP Proteine)] in the remaining samples

  10. Copy number variations in alpha-globin (zeige HBA1 Proteine) 2 gene is associated with increased levels of HbF with beta thalassemia.

HBa2 Protein Überblick

Protein Überblick

The human alpha globin gene cluster located on chromosome 16 spans about 30 kb and includes seven loci: 5'- zeta - pseudozeta - mu - pseudoalpha-1 - alpha-2 - alpha-1 - theta - 3'. 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.

Genbezeichner und Symbole assoziert mit Hemoglobin, alpha 2 Proteine (HBa2)

  • hemoglobin, alpha 2 (Hba2)
  • alpha-D-globin (HBAD)
  • hemoglobin, alpha 2 (HBA2)
  • hemoglobin, alpha 2 (hba2)
  • HBA2 Protein
  • hba5 Protein
  • HBH Protein

Bezeichner auf Proteinebene für Hemoglobin, alpha 2 Proteine (HBa2)

2-alpha globin , 2-alpha-1 globin , hemoglobin alpha 2 chain , adult alpha D globin , hemoglobin alpha-D chain , hemoglobin subunit alpha-D , hemoglobin, alpha 2 , hemoglobin subunit alpha , globin, alpha 2 , hemoglobin, subunit alpha 2 , alpha globin , alpha-2 globin , alpha-globin , hemoglobin alpha chain , alpha T5 (aa 1-142) , alpha-5-globin , alpha-T5 , hemoglobin alpha-5 chain , hemoglobin subunit alpha-5

360504 Rattus norvegicus
416651 Gallus gallus
100036558 Equus caballus
3040 Homo sapiens
379435 Xenopus laevis
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