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Calcyphosine 2 抗体 (AA 221-320) (Biotin)

This Biotin-conjugated 兔 多克隆 anti-Calcyphosine 2 antibody specifically detects Calcyphosine 2 in ELISA, IHC (p) 和 IHC (fro). The antibody is reactive with 人 samples.
产品编号 ABIN1395523
发货至: 中国
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Quick Overview for Calcyphosine 2 抗体 (AA 221-320) (Biotin) (ABIN1395523)

抗原

See all Calcyphosine 2 (CAPS2) 抗体
Calcyphosine 2 (CAPS2)

适用

  • 30
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  • 1

宿主

  • 30
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克隆类型

  • 30
  • 3
多克隆

标记

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  • 2
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  • 1
  • 1
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This Calcyphosine 2 antibody is conjugated to Biotin

应用范围

  • 13
  • 13
  • 10
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  • 1
ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • 抗原表位

    • 14
    • 5
    • 1
    • 1
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    • 1
    • 1
    AA 221-320

    预测反应

    Human,Mouse,Rat,Cow,Sheep,Pig,Chicken

    纯化方法

    Purified by Protein A.

    免疫原

    KLH conjugated synthetic peptide derived from human Calcyphosine 2/CAPS2

    亚型

    IgG
  • 应用备注

    IHC-P 1:200-400
    IHC-F 1:100-500

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 μg/μL

    缓冲液

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % 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

    -20 °C

    储存方法

    Store at -20°C for 12 months.

    有效期

    12 months
  • 抗原

    Calcyphosine 2 (CAPS2)

    别名

    Calcyphosine 2/CAPS2

    背景

    Synonyms: Calcyphosin 2, Calcyphosin-2, Calcyphosine-2, Calcyphosine2, Calcyphosphine 2, CAPS 2, CAPS2, CAYP2_HUMAN, D630005B03Rik, FLJ34520, OTTHUMP00000202412, OTTMUSP00000027695, UG0636c06.

    Background: CAPS2 is a 557 amino acid calcium-binding protein that is abundantly expressed, with highest expression found in placenta, testis, colon, lung and brain. CAPS2 contains three EF-hand domains and exists as three alternatively spliced isoforms. Suggested to play a role in large dense-core vesicle (LDCV) exocytosis, CAPS2 is encoded by a gene that maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.

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