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The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. Zusätzlich bieten wir Ihnen Hemoglobin Subunit beta Proteine (200) und Hemoglobin Subunit beta Kits (28) und viele weitere Produktgruppen zu diesem Protein an.
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Human Monoclonal Hemoglobin Subunit beta Primary Antibody für ELISA, WB - ABIN561229
Xie, Ren, Zhang, Guo, Wang, Wang, Lin, Gong, Li, Huang, Zeng, Zeng: Restoration of the balanced alpha/beta-globin gene expression in beta654-thalassemia mice using combined RNAi and antisense RNA approach. in Human molecular genetics 2007
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Human Monoclonal Hemoglobin Subunit beta Primary Antibody für IHC (p), ELISA - ABIN561230
Ishikawa, Ohlmeier, Salmenkivi, Myllärniemi, Rahman, Mazur, Kinnula: Hemoglobin ? and ? are ubiquitous in the human lung, decline in idiopathic pulmonary fibrosis but not in COPD. in Respiratory research 2010
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Human Polyclonal Hemoglobin Subunit beta Primary Antibody für ELISA, WB - ABIN561228
Martins, Rino, Carvalho, Carvalho, Yoshida, Klose, de Almeida, Carmo-Fonseca: Spliceosome assembly is coupled to RNA polymerase II dynamics at the 3' end of human genes. in Nature structural & molecular biology 2011
Pan (zeige SUPT6H Antikörper) troglodytes and Pongo pygmaeus were screened for mutations in the beta-globin gene (exons 1, 2, and 3) for suspected thalassemia.
We found no evidence of the major deleterious mutations at HBB in chimpanzees that confer resistance to malaria caused by Plasmodium falciparum nor evidence of long-term balancing selection at these loci.
Data indicate that on incubating hemoglobin with glyoxal for 0-20 days, advanced glycation end products (AGEs) were detected on day 20.
In this study, hemoglobin subunit beta was identified as a classical swine fever virus capsid protein-binding protein by glutathione S-transferase (zeige GSTa2 Antikörper) pulldown and subsequent mass spectrometry analysis of PK-15 cells.
human bone marrow stromal cells-derived induced pluripotent stem sacs allow for more efficient erythroid cell generation with higher beta-globin production, likely due to heightened emergence of immature progenitors.
study reports 3 novel HBB mutations - one in the promoter (-90 C>G), a 20 bp deletion in exon 2 (FS Cd 78/85) and a mutation in the donor site of intron 2 (IVS2:2 T>G); considering these novel mutations and the first observation of IVS1:6T>C, the molecular spectrum of beta-thalasemia in Mexicans comprises 21 different mutations, confirming the high allelic heterogeneity in Mexicans
Embryonic stem cell sacs serve as hemangioblast-like progenitors capable to generate definitive erythroid cells that express beta-globin.
In the presence of free alpha subunits and H2O2, both HbA (zeige SCN2A Antikörper) and HbE (zeige HBe1 Antikörper) showed bCys93 oxidation which increased with higher H2O2 concentrations. In the presence of Alpha-hemoglobin stabilizing protein (AHSP (zeige aHSP Antikörper))Cys93 oxidation was substantially reduced in both proteins.in the presence of excess free alpha-subunit (zeige POLG Antikörper) and under the same oxidative conditions, these events are substantially increased for HbE (zeige HBe1 Antikörper) compared to HbA (zeige SCN2A Antikörper)
In conclusion, in this work we demonstrated that HBB is expressed by breast cancer cells, its expression is correlated with tumour aggressiveness in humans and its forced overexpression enhances breast cancer cell aggressiveness in vitro and in vivo.
NF-E2 (zeige NFE2 Antikörper), TAL1 (zeige TAL1 Antikörper) and KLF1 (zeige KLF1 Antikörper), all activators play a primary role in HSs (zeige GFER Antikörper) formation in the LCR
Five different beta-globin haplotypes were linked to sickle hemoglobin alleles in Mazandaran province.
2 cases of Polish patients with hereditary hemolytic anemia suspected of thalassemia were studied; identified 2 different frameshift mutations positioned in the third exon of HBB; results show a lack of natural stop codon due to the frameshift in exon 3 of beta-globin gene causes rapid degradation of its mRNA and indicate existence of novel surveillance pathway
Our work suggested a novel function for HBB as a theranostic molecule: an innate antimetastasis factor with potential utility as an anticancer drug and a biomarker signaling the presence of clinically undetectable metastasis
we concluded that this novel beta-globin gene mutation was associated with the mild phenotype of beta-thal.
Data show that mediator is recruited to the beta-globin locus by the LDB1 (zeige LDB1 Antikörper) complex.
In hemizygous beta-globin knockout (BKO) mice, the duodenal calcium transport was lower than that in wild-type littermates, and severity was especially pronounced in female mice.
The study analyzed protein-DNA interactions in the murine beta-globin gene locus.
Data suggest that beta-globin promoters in general do not exert any appreciable nonlocal effects on chromatin structure.
HIRA (zeige HIRA Antikörper) is not only critical for beta-globin expression but is also required for activation of the erythropoietic regulators EKLF (zeige KLF1 Antikörper) and GATA binding protein 1 (GATA1).
Data indicate that Myb and BCL11A cooperate with DNMT1 to achieve developmental repression of embryonic and fetal beta-like human transgenic globin genes in the adult erythroid environment.
A single observed change in a histocompatibility complex (MHC) peptide (I-Ek) anchor residue historically induces a different topology at an important segment of hemoglobin beta chain peptide bound to a T-cell receptor amino acid residue.
GATA-1 (zeige GATA1 Antikörper) occupies the beta-major globin promoter normally in fetal liver erythroblasts from mice lacking the LCR, suggesting that GATA-1 (zeige GATA1 Antikörper) binding to the promoter and LCR are independent events that occur prior to loop formation.
These results are consistent with the hypothesis that activation of the beta-globin gene locus is initiated by protein complexes recruited to the LCR.
Reactive beta globin sulfhydryl group concentration is genetically determined.
The alpha (HBA) and beta (HBB) loci determine the structure of the 2 types of polypeptide chains in adult hemoglobin, Hb A. The normal adult hemoglobin tetramer consists of two alpha chains and two beta chains. Mutant beta globin causes sickle cell anemia. Absence of beta chain causes beta-zero-thalassemia. Reduced amounts of detectable beta globin causes beta-plus-thalassemia. The order of the genes in the beta-globin cluster is 5'-epsilon -- gamma-G -- gamma-A -- delta -- beta--3'.
, hemoglobin beta chain
, hemoglobin subunit beta
, beta globin
, hemoglobin beta-1/2 chain
, hemoglobin subunit beta-1/2
, Hemoglobin beta chain
, globin, beta
, hemoglobin beta
, beta globin chain
, III beta-1 globin
, III beta-2 globin
, hemoglobin beta chain complex
, hemoglobin beta chain, major-form
, hemoglobin beta-1 chain
, hemoglobin subunit beta-1