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Act as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Additionally we are shipping aHSP Antibodies (46) and aHSP Proteins (18) and many more products for this protein.
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Findings indicate that alpha-hemoglobin-stabilizing protein (AHSP) expression is a biomarker of hemoglobin (show HBB ELISA Kits) H (HbH (show HBA1 ELISA Kits)) disease severity and infer an important role of AHSP in modulating the pathophysiology of this disease.
AHSP is predominantly expressed in erythroid precursors in bone marrow biopsy specimens from patients with hematologic malignancies.
AHSP expression was higher in patients with sickle cell anemia versus thalassemia, with no significant difference between BTM and BTI. Expression was higher in patients with NTDT and on hydroxyurea therapy.
In maturing RBC (show CACNA1C ELISA Kits) progenitors AHSP bind to free alpha-globin (show HBA1 ELISA Kits) chains to increase the HbA (show SCN2A ELISA Kits) production. (Review)
analysis showed binding of STAT3 (show STAT3 ELISA Kits) to AHSP promoter and binding was significantly augmented with IL6 (show IL6 ELISA Kits) stimulation and upon alpha-globin (show HBA1 ELISA Kits) overexpression
The relationship between AHSP gene expression, disease severity, and the beta/alpha globin (show HBA1 ELISA Kits) mRNA ratio was studied among different homozygote beta-thalassemia patients.
alpha-Hemoglobin-stabilizing protein (AHSP) perturbs the proximal heme pocket of oxy (show GCG ELISA Kits)-alpha-hemoglobin and weakens the iron-oxygen bond.
alpha-Hemoglobin stabilizing protein (AHSP) markedly decreases the redox potential and reactivity of alpha-subunits of human HbA (show SCN2A ELISA Kits) with hydrogen peroxide.
AHSP acts as a molecular chaperone (show HSP90AA1 ELISA Kits) by rapidly binding and stabilizing met-alpha hemichrome folding intermediates
AHSP could be a secondary compensatory mechanism in red blood cells to counterbalance the excess of alpha-globin (show HBA1 ELISA Kits) chains in HbE (show HBe1 ELISA Kits)/beta-thalassaemia individuals.
role of alpha-hemoglobin stabilizing protein in hemoglobin assembly
Endogenous AHSP is not limiting for alpha-globin (show HBA-A1 ELISA Kits) detoxification in beta-thalassemic mice.
activin A (show INHBA ELISA Kits) does not appear to affect the exocrine or endocrine components of the pancreas, but promotes differentiation of pancreatic tissue into intestine via a Shh (show SHH ELISA Kits)-dependent mechanism
Loss of AHSP impairs erythropoiesis and exacerbates beta-thalassemia.
These results support the hypothesis that EKLF (show KLF1 ELISA Kits) acts as a transcription factor and a chromatin modulator for the AHSP and beta-globin (show HBB ELISA Kits) genes and indicate that EKLF (show KLF1 ELISA Kits) may play similar roles for other erythroid genes.
developmental stage- and differentiation state-specific regulation of the nuclear transport of EKLF (show KLF1 ELISA Kits) might be one of the steps necessary for the switch-on of the mammalian adult beta globin (show HBB ELISA Kits) gene transcription
AHSP also acts as a molecular chaperone to stabilize nascent alpha-globin for hemoglobin A assembly
The expression of AHSP in a subclone of murine erythroleukemia cells in relationship to prion protein (show PRNP ELISA Kits) on the cell surface is reported.
Act as a chaperone to prevent the harmful aggregation of alpha-hemoglobin during normal erythroid cell development. Specifically protects free alpha-hemoglobin from precipitation (By similarity).
alpha hemoglobin stabilizing protein
, erythroid associated factor
, alpha hemoglobin stabilising protein
, alpha-hemoglobin-stabilizing protein
, erythroid differentiation associated factor
, erythroid differentiation-related factor
, erythroid-associated factor