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The gamma globin genes (HBG1 and HBG2) are normally expressed in the fetal liver, spleen and bone marrow. Additionally we are shipping HBG2 Kits (29) and HBG2 Proteins (8) and many more products for this protein.
Showing 10 out of 22 products:
Human Polyclonal HBG2 Primary Antibody for WB - ABIN1944849
Ota, Suzuki, Nishikawa, Otsuki, Sugiyama, Irie, Wakamatsu, Hayashi, Sato, Nagai, Kimura, Makita, Sekine, Obayashi, Nishi, Shibahara, Tanaka, Ishii, Yamamoto, Saito, Kawai, Isono, Nakamura, Nagahari et al.: Complete sequencing and characterization of 21,243 full-length human cDNAs. ... in Nature genetics 2003
Show all 4 Pubmed References
Human Polyclonal HBG2 Primary Antibody for WB - ABIN1944740
Slightom, Blechl, Smithies: Human fetal G gamma- and A gamma-globin genes: complete nucleotide sequences suggest that DNA can be exchanged between these duplicated genes. in Cell 1981
Show all 4 Pubmed References
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 (show HBe1 Antibodies), MCV and MCH (show PMCH Antibodies) levels in Thai HbE (show HBe1 Antibodies) 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 (show BCL11A Antibodies) 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.
Our data suggest that a temporal repression mechanism is operative in the silencing of gamma-globin gene expression
results establish SATB2 as a novel gamma-globin gene regulator and provide a glimpse of the differential and cooperative roles of SATB family proteins in modulating clustered genes transcription
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