Human Hemoglobin subunit delta(HBD) ELISA kit
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中文名称:人血红蛋白δ亚基(HBD)酶联免疫试剂盒
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货号:CSB-EL010152HU
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规格:96T/48T
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价格:¥3600/¥2500
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其他:
产品详情
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产品描述:
This Human HBD ELISA Kit was designed for the quantitative measurement of Human HBD protein in serum, plasma, lysate for RBC.. It is a Competitive ELISA kit, its detection range is 0.007 ng/mL-30 ng/mL and the sensitivity is 0.007 ng/mL.
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别名:Delta-globin ELISA Kit; HBD ELISA Kit; HBD_HUMAN ELISA Kit; Hemoglobin delta chain ELISA Kit; Hemoglobin subunit delta ELISA Kit
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缩写:
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Uniprot No.:
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种属:Homo sapiens (Human)
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样本类型:serum, plasma, lysate for RBC.
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检测范围:0.007 ng/mL-30 ng/mL
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灵敏度:0.007 ng/mL
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反应时间:1-5h
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样本体积:50-100ul
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检测波长:450 nm
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研究领域:Signal Transduction
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测定原理:quantitative
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测定方法:Competitive
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数据处理:
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货期:3-5 working days
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靶点详情
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功能:Involved in oxygen transport from the lung to the various peripheral tissues.
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基因功能参考文献:
- Blood donor homozygous for Hb D Los Angeles. PMID: 25217459
- The expression of the activated delta-globin gene in a beta-thalassemia mice model greatly improves the phenotype, validating the delta-globin chain as a therapeutic target for beta-hemoglobinopathies. PMID: 23872310
- Data indicate that a delta-globin mutation was suspected in both patients. PMID: 23806011
- Twenty-one different mutations were detected, and of these 12 have not been previously described. PMID: 23215833
- A functional promoter polymorphism of the delta-globin gene is a specific marker of the Arab-Indian haplotype PMID: 22641479
- This report describes a novel missense mutation in delta-globin (HBD: c.323G>A, Gly > Asp) in an Indian family with heterozygous beta-thalassemia with normal HbA(2) levels. PMID: 22477537
- The 5' breakapoint of the (deltabeta)(0) thalassemia deletion in a compound heterozygote was located in the second intron of the delta globin gene. PMID: 11860449
- Hb A2-Monreale [delta146(HC3)His-->Arg]is a novel delta chain variant. PMID: 11939506
- alternate mRNA species in adult erythroid cells; mRNA encodes an additional 145 nt in the upstream untranslated region, suggesting an alternative site of transcriptional initiation and transcription through the previously defined promoter PMID: 15234005
- The atomic coordinates of the delta-chain of hemoglobin A2 (R2 state) are used to model the structure of hemoglobin homotetramer delta 4, which occurs in rare hemoglobin H disease. PMID: 15449937
- Deletion pf this geneis a common, and possibly the predominant beta-thalassemia mutation of the Austroasiatic Lao Theung population. PMID: 15757827
- characterization of the delta-globin gene alleles and of RFLP-haplotypes, SNPs and one microsatellite associated with them in 231 carriers originating principally from East Sicily; Seventeen alleles were identified, of which five were new PMID: 18221842
- Borderline HbA(2) is not a rare event in a population with a high prevalence of beta-thalassemia carriers PMID: 18603555
- Unusually low levels of HBA2 in a compound heterozygote can be explained from the functional inhibition of the HBD gene, in cis to the HBG1 gene, bearing the nd-HPFH mutation. PMID: 18615450
- Hb A2 IVS-I-5 (G > C) beta-thalassemia mutation phenotype in 289 carriers was reported. PMID: 18932068
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蛋白家族:Globin family
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组织特异性:Red blood cells.
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数据库链接:
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