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The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Zusätzlich bieten wir Ihnen HBG2 Antikörper (25) und HBG2 Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.
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Data suggest that studying genotype frequency of the Xmn1 gammaG globin polymorphism (-158C>T ) in Siwa Oasis, Egypt can be considered as a starting point for further research targeting this community sector.
The results suggested that there was a significant relationship between high fetal hemoglobin levels and two variations (-309A/T and -369C/G) in Ggamma gene promotor.
Genetic association studies provide a rationale for functional studies of HBG2 expression in wild-type and T/A/T haplotype erythroblasts and mechanistic studies like chromatin conformation capture experiments, to evaluate the role of chromatin looping as a mediator of the T/A/T haplotype effects on HbF.
In Portuguese beta-thalassemia carriers the HBG2 XmnI polymorphism is strongly associated with HbF levels.
DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
Its polymorphism effects HbF, HbE (zeige HBe1 ELISA Kits), MCV and MCH (zeige PMCH ELISA Kits) levels in Thai HbE (zeige HBe1 ELISA Kits) carriers.
Data indicate that the T to A conversion results in a leucine to histidine amino acid change at codon 105 of the (G)gamma-globin HBG2 gene and caused a hemoglobin (Hb) variant with lowered oxygen affinity.
Hemoglobin gamma G plays a role in modifying clinical symptoms of beta-thalassemia innorthern Thailand.
Data suggest that segregation of BCL11A (zeige BCL11A ELISA Kits) haplotype 2 indicating an involvement of this locus in Hb F expression.
Hb F is regulated in inherited bone marrow failure syndromes by Xmn1-HBG2, as it is in the haemoglobinopathies.
The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Two gamma chains together with two alpha chains constitute fetal hemoglobin (HbF) which is normally replaced by adult hemoglobin (HbA) at birth. In some beta-thalassemias and related conditions, gamma chain production continues into adulthood. The two types of gamma chains differ at residue 136 where glycine is found in the G-gamma product (HBG2) and alanine is found in the A-gamma product (HBG1). The former is predominant at birth. The order of the genes in the beta-globin cluster is: 5'- epsilon -- gamma-G -- gamma-A -- delta -- beta--3'.
G-gamma globin Paulinia
, abnormal hemoglobin
, hb F Ggamma
, hemoglobin gamma-2 chain
, hemoglobin gamma-G chain
, hemoglobin subunit gamma-2
, hemoglobin, gamma G
, gamma-2 globin
, Hemoglobin subunit gamma-1