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HBA1 抗体 (AA 2-142) (FITC)

The FITC-conjugated 兔 多克隆 anti-HBA1 antibody (ABIN7996907) specifically detects HBA1 in FACS. The antibody is reactive with 人 samples.
产品编号 ABIN7996907
发货至: 中国
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Quick Overview for HBA1 抗体 (AA 2-142) (FITC) (ABIN7996907)

抗原

See all HBA1 抗体
HBA1 (Hemoglobin, alpha 1 (HBA1))

适用

  • 67
  • 31
  • 15
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宿主

  • 69
  • 9

克隆类型

  • 51
  • 27
多克隆

标记

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This HBA1 antibody is conjugated to FITC

应用范围

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Flow Cytometry (FACS)
  • 抗原表位

    • 24
    • 9
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    • 2
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    AA 2-142

    原理

    Anti-Hemoglobin/HBA1/HBA2 Antibody FITC Conjugated

    特异性

    No cross reactivity with other proteins.

    交叉反应 (详细)

    No cross-reactivity with other proteins

    预测反应

    Human Hemoglobin shares 85.8% amino acid (aa) sequence identity with mouse Hemoglobin.

    纯化方法

    Immunogen affinity purified.

    免疫原

    E.coli-derived human Hemoglobin recombinant protein (Position: V2-R142). Human Hemoglobin shares 85.8% amino acid (aa) sequence identity with mouse Hemoglobin.

    亚型

    IgG
  • 应用备注

    Flow Cytometry, Optimal dilutions should be determined by end users.

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

    储存液

    Sodium azide

    注意事项

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    储存条件

    -20 °C

    储存方法

    At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

    有效期

    12 months
  • 抗原

    HBA1 (Hemoglobin, alpha 1 (HBA1))

    别名

    HBA1

    背景

    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.

    Gene Full Name: hemoglobin subunit alpha 1

    基因ID

    3039, 3040

    UniProt

    P69905
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