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Hemoglobin Alpha 1 + 2 (HBA1,HBA2) (AA 10-60) 抗体

HBA1,HBA2 适用: 人, 小鼠 IHC (p), IF (p) 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN1387969
发货至: 中国
  • 抗原 See all Hemoglobin Alpha 1 + 2 (HBA1,HBA2) 抗体
    Hemoglobin Alpha 1 + 2 (HBA1,HBA2)
    抗原表位
    • 7
    • 1
    • 1
    AA 10-60
    适用
    • 12
    • 10
    • 1
    人, 小鼠
    宿主
    • 15
    克隆类型
    • 15
    多克隆
    标记
    • 4
    • 3
    • 3
    • 3
    • 1
    • 1
    非结合性
    应用范围
    • 15
    • 13
    • 10
    • 7
    • 5
    • 1
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
    交叉反应
    人, 小鼠
    纯化方法
    Purified by Protein A.
    免疫原
    KLH conjugated synthetic peptide derived from human Hemoglobin alpha
    亚型
    IgG
  • 应用备注
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    限制
    仅限研究用
  • 状态
    Liquid
    浓度
    1 μg/μL
    缓冲液
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    储存液
    ProClin
    注意事项
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    储存条件
    4 °C,-20 °C
    储存方法
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    有效期
    12 months
  • 抗原
    Hemoglobin Alpha 1 + 2 (HBA1,HBA2)
    别名
    HBA1+HBA2 (HBA1,HBA2 产品)
    别名
    HBAM antibody, Hba-a1 antibody, Hba-a2 antibody, CD31 antibody, HBH antibody, Hba antibody, Hba1 antibody, Hbat1 antibody, hemoglobin, alpha 1 antibody, hemoglobin subunit alpha 1 antibody, hemoglobin alpha, adult chain 1 antibody, Hba1 antibody, HBA1 antibody, Hba-a1 antibody
    背景

    Synonyms: HBH, HBA-T3, Hemoglobin subunit alpha, Alpha-globin, Hemoglobin alpha chain, HBA1

    Background: 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. [provided by RefSeq, Jul 2008].

    基因ID
    3039
    UniProt
    P69905
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