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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'. 再加上，我们可以发HBa2 抗体 (15) 和 HBa2 蛋白 (6)和数多这个蛋白质的别的产品。
Carriers of Hb Nanning are asymptomatic and could be missed by screening based on MCV and MCH (显示 PMCH ELISA试剂盒) cutoffs of <80.0 fL and <27.0 pg, respectively. Both carriers of the mutation in the study have MCV and MCH (显示 PMCH ELISA试剂盒) values that are 2 standard deviations (SDs (显示 SDS ELISA试剂盒)) below normal, as would be predicted for an alpha+-thal.
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 (显示 VWF ELISA试剂盒)) or type I collagen under shear stresses.
Hb Adana mutation was preferentially present in the alpha2-globin genes in Malays compared to the other ethnicities in Malaysia.
Seven novel nondeletional alpha-thalassemia mutations localized on the alpha2-globin gene in the heterozygous state were identified
Gene frequency for HBA2:c.301-24delGinsCTCGGCCC carriers among the Chinese population in Guangxi.
Hemoglobin Constant Spring mutation in Southeast Asians with thalassemia.
We report herein for the first time the description of HbA2' in the Tunisian population.
In maturing RBC (显示 CACNA1C ELISA试剂盒) progenitors AHSP (显示 aHSP ELISA试剂盒) bind to free alpha-globin (显示 HBA1 ELISA试剂盒) chains to increase the HbA (显示 SCN2A ELISA试剂盒) production. (Review)
Two mutations detected the -a(3,7) single gene deletion found in 75% of cases and the nongene deletion a2 IVS1 [-5nt (显示 ACPP ELISA试剂盒)] in the remaining samples
Copy number variations in alpha-globin (显示 HBA1 ELISA试剂盒) 2 gene is associated with increased levels of HbF with beta thalassemia.
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.
, 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
, hemoglobin alpha chain
, alpha T5 (aa 1-142)
, hemoglobin alpha-5 chain
, hemoglobin subunit alpha-5