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NECAB1 抗体

The 小鼠 单克隆 anti-NECAB1 antibody is suitable to detect NECAB1 in samples from 人. It has been validated for WB 和 IHC (p).
产品编号 ABIN7881751
发货至: 中国
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Quick Overview for NECAB1 抗体 (ABIN7881751)

抗原

See all NECAB1 抗体
NECAB1 (N-terminal EF-Hand Calcium Binding Protein 1 (NECAB1))

适用

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宿主

  • 22
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小鼠

克隆类型

  • 24
  • 16
单克隆

标记

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This NECAB1 antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

Carrier-free

克隆位点

NECAB1-7680
  • 原理

    NECAB1 Antibody / N-terminal EF-hand calcium binding protein 1 (azide and preservative free)

    纯化方法

    Protein A/G affinity

    免疫原

    Recombinant human NECAB1 protein was used as the immunogen for the NECAB1 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the NECAB1 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    -20 °C

    储存方法

    Aliquot the NECAB1 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
  • 抗原

    NECAB1 (N-terminal EF-Hand Calcium Binding Protein 1 (NECAB1))

    别名

    NECAB1

    背景

    Members of the EF-CBP (N-terminal EF-hand calcium binding protein)/NECAB (neuronal calcium-binding protein) family participate in neuronal calcium signaling. EF-CBP1 (N-terminal EF-hand calcium binding protein 1), also known as STIP-1 or neuronal calcium-binding protein 1 (NECAB1), is a 351 amino acid cytoplasmic protein that contains one antibiotic biosynthesis monooxygenase (ABM) domain and 2 EF-hand domains. Expressed in brain, EF-CBP1 interacts with copine 6 and Syntaxin, and exists as two alternatively spliced isoforms. The gene encoding EF-CBP1 maps to human chromosome 8, which consists of nearly 146 million base pairs, encodes over 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.

    UniProt

    Q8N987
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