Hemoglobin, alpha 1 (HBA1) ELISA试剂盒

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Hemoglobin, alpha 1 抗体 (52)Hemoglobin, alpha 1 蛋白 (28)和数多这个蛋白质的别的产品。

list all ELISA KIts 基因 基因ID UniProt
HBA1 25632 P01946
HBA1 3039 P69905
HBA1 15122  
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引用最多的Hemoglobin, alpha 1 ELISA试剂盒

  1. Rat (Rattus) HBA1 ELISA Kit for Sandwich ELISA - ABIN457240 : Yao, Li, Gao, Pallua, Steffens: Improving the angiogenic potential of collagen matrices by covalent incorporation of Astragalus polysaccharides. in International journal of burns and trauma 2012 (PubMed)
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适于 Hemoglobin, alpha 1 相互作用对的更多 ELISA 试剂盒

Horse (Equine) Hemoglobin, alpha 1 (HBA1) interaction partners

  1. This study presents comparison of two neutron structures of hemoglobins, human deoxyhemoglobin (T state) and equine cyanomethemoglobin (R state) and offers a direct observation of histidine residues that are likely to contribute to the Bohr effect.

  2. cyanomethemoglobin is in the R state and preliminary room-temperature electron and neutron scattering density maps clearly show the protonation states of potential Bohr groups.

Human Hemoglobin, alpha 1 (HBA1) interaction partners

  1. In this new nonsense mutation, short genetic products may suffer nonsense-mediated degradation, whereas the abnormal protein will be eliminated through the proteolytic pathway mediated by ubiquitin

  2. Relatively high but clinically normal HbA1c and TSH levels may increase the risk of CHD.

  3. Vaginal cell-derived Hb-alpha and Hb-beta may have antioxidative properties and protect cells from oxidative stress-induced inflammation possibly through Nrf2 downstream signaling.

  4. Data suggest that, in crystal form of Hb containing three protein molecules--Hbalpha(1)beta(2), allosteric effectors (phosphate, bezafibrate) induce conformational changes in direction from relaxed-state to tense-state; binding of each effector energetically stabilizes lowest affinity conformer more strongly than intermediate affinity conformer; minor Hb conformers have disproportionate effects on overall O(2) affinity.

  5. In the presence of free alpha subunits and H2O2, both HbA and HbE showed bCys93 oxidation which increased with higher H2O2 concentrations. In the presence of Alpha-hemoglobin stabilizing protein (AHSP)Cys93 oxidation was substantially reduced in both proteins.in the presence of excess free alpha-subunit and under the same oxidative conditions, these events are substantially increased for HbE compared to HbA

  6. genome-wide association meta-analyses in individuals from 82 cohorts of European, African, East Asian and South Asian ancestry; identified 60 common genetic variants associated with HbA1c; 19 glycemic (GS-G) and 22 erythrocytic (GS-E) variants were associated with HbA1c at genome-wide significance; GS-G was associated with higher type 2 diabetes risk; GS-E was not

  7. This study presents comparison of two neutron structures of hemoglobins, human deoxyhemoglobin (T state) and equine cyanomethemoglobin (R state) and offers a direct observation of histidine residues that are likely to contribute to the Bohr effect.

  8. Dynamical differences of hemoglobin and the ionotropic glutamate receptor in different states have been revealed by a new dynamics alignment method.

  9. The studies suggest that impaired endocytosis of megalin/cubilin ligands, hemoglobin and albumin, rather than heme toxicity, may be the cause of tubular proteinuria in sickle cell disease patients.

  10. Report association between HbA1c levels in diabetes mellitus type 2 in relation to the development of heart failure.

  11. Lower extremity amputation among patients with diabetes nearly halved over the past decade but only weakly correlated with hemoglobin A1c testing throughout the study period.

  12. 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) or type I collagen under shear stresses.

  13. A 1 % increase in HbA1c was associated with a higher risk for all-cause mortality in patients with type 2 diabetes and symptomatic cardiovascular disease

  14. 14 alpha thalassemia mutations were found among 95 Turkish patients. Most were gene deletions. A new alpha 1 cd 14 mutation was discovered.

  15. The hematological and molecular data of 35 patients with Hb H disease and the genotypes of alpha-gene mutations of 78 screened individuals were used to identify the genotypes of Hb H disease and genotype-phenotype correlations. the most common genotypes were -alpha3.7/--20.5, -alpha3.7/--26.5, and -alpha3.7/--17.5. Other small deletions, non-deleltional mutations, and combinations thereof in trans were associated with...

  16. that there is a quantitative relationship between the HbA1c levels and plaque textures in ultrasonic images of atherosclerotic patients

  17. An association has been found between the TXNIP gene methylation pattern and type 2 diabetes mellitus in ischemic stroke patients through epigenetic mechanisms, related to sustained hyperglycemia levels with HbA1c >/= 7%.

  18. People with new-onset diabetes mellitus based on HbA1c had higher mean hs-CRP level.

  19. This study describes hematological manifestations of subjects carrying some novel mutations comparable to the reported phenotype of alpha(+)-thal trait.

  20. The effect of the DPP-4 inhibitor alogliptin on HbA1c.

Mouse (Murine) Hemoglobin, alpha 1 (HBA1) interaction partners

  1. identify a novel sequence on Hb alpha that is important for Hb alpha/eNOS complex formation and is critical for nitric oxide signaling at myoendothelial junctions

  2. Because haemoglobin regulates O2 and/or nitric oxide availability, it may contribute to regulation of these gases during the ovulatory period in vivo.

  3. The human locus establishes prominent sites of Polycomb complex recruitment in pluripotent stem cells, whereas the corresponding mouse locus does not.

  4. Allosteric effects of chloride ions at the interfaces between the alphabeta dimers.

  5. The objective of this study was to test whether amino acid differences among triplicated alpha-globin paralogs are attributable to a relaxation of purifying selection or to a history of positive selection.

  6. It is suggested that the higher expression of hemoglobin alpha1 in the brain may be associated with ECM and could be a source of excess heme, a molecule that is considered to trigger the pathogenesis of cerebral malaria.

  7. These data suggest that CP2b potentiate erythroid cell-specific alpha-globin expression by recruiting CP2c into the nucleus.

Rabbit Hemoglobin, alpha 1 (HBA1) interaction partners

  1. A comparative study of tetrameric rabbit hemoglobin and monomeric soybean leghemoglobin a in the oxy- and deoxy-forms was carried out using (57)Fe Mossbauer spectroscopy

Zebrafish Hemoglobin, alpha 1 (HBA1) interaction partners

  1. Joint locus of alpha/beta-globin genes in Danio rerio is segregated into structural subdomains active at different stages of development.

Hemoglobin, alpha 1 (HBA1) 抗原简介

Antigen Summary

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.

Gene names and symbols associated with HBA1

  • hemoglobin, alpha 1 (HBA) 抗体
  • hemoglobin, alpha 1 (Hba1) 抗体
  • hemoglobin subunit alpha 1 (hba1) 抗体
  • hemoglobin subunit alpha 1 S homeolog (hba1.S) 抗体
  • hemoglobin, alpha 1 (HBA1) 抗体
  • hemoglobin, alpha 2 (HBA1) 抗体
  • hemoglobin subunit alpha 1 (HBA1) 抗体
  • hemoglobin alpha, adult chain 1 (Hba-a1) 抗体
  • alpha-hemoglobin (HBA) 抗体
  • hemoglobin, alpha adult 1 (hbaa1) 抗体
  • hemoglobin subunit alpha-2-like (LOC102168959) 抗体
  • AA1 抗体
  • CD31 抗体
  • dZ118J2.2 抗体
  • Hba 抗体
  • hba-a 抗体
  • Hba-a1 抗体
  • Hba-a2 抗体
  • Hba1 抗体
  • HBA2 抗体
  • HBAI 抗体
  • HBAII 抗体
  • HBAM 抗体
  • Hbat1 抗体
  • HBH 抗体

Protein level used designations for HBA1

alpha-globin , globin, alpha 1 , hemoglobin alpha chain , hemoglobin subunit alpha , alpha-1/2-globin , hemoglobin alpha 1 chain , hemoglobin alpha, adult chain 1 , hemoglobin alpha, adult chain 2 , hemoglobin alpha-1/2 chain , hemoglobin subunit alpha-1/2 , X.tropicalis alpha globin , alpha globin adult , hemoglobin subunit alpha-2 , alpha-2-globin chain , hemoglobin alpha-2 chain , hemoglobin alpha-minor chain , hemoglobin, alpha 1 , alpha 2 globin , alpha one globin , alpha-1 globin , alpha-1-globin , hemoglobin alpha 1 globin chain , hemoglobin alpha-1 chain , alpha 1 globin , alpha globin 1 , haemaglobin alpha 1 , alpha-globin 1 , alpha-globin aa1 , Alpha-1-globin , Alpha-2-globin , Hemoglobin alpha-1 chain , Hemoglobin alpha-2 chain , Hemoglobin subunit alpha-1 , Hemoglobin subunit alpha-2 , I alpha globin , II alpha globin , hemoglobin subunit alpha-1 , Alpha-globin , Hemoglobin alpha chain

GENE ID SPECIES
100036557 Equus caballus
25632 Rattus norvegicus
394454 Xenopus (Silurana) tropicalis
397869 Xenopus laevis
100137279 Papio anubis
732486 Pan troglodytes
3039 Homo sapiens
15122 Mus musculus
100009249 Oryctolagus cuniculus
30507 Danio rerio
102168959 Capra hircus
100140149 Bos taurus
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