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ADAM22 抗体 (Extracellular, N-Term)

This 兔 多克隆 antibody specifically detects ADAM22 in WB, IHC 和 IF. It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7884717
发货至: 中国
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Quick Overview for ADAM22 抗体 (Extracellular, N-Term) (ABIN7884717)

抗原

See all ADAM22 抗体
ADAM22 (ADAM Metallopeptidase Domain 22 (ADAM22))

适用

  • 22
  • 15
  • 7
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
人, 小鼠, 大鼠

宿主

  • 18
  • 11
  • 1
  • 1

克隆类型

  • 16
  • 15
多克隆

标记

  • 23
  • 2
  • 2
  • 2
  • 2
This ADAM22 antibody is un-conjugated

应用范围

  • 21
  • 14
  • 13
  • 10
  • 6
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)

质量等级

Carrier-free
  • 抗原表位

    • 7
    • 6
    • 6
    • 6
    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 715-729, Extracellular, N-Term

    原理

    A Rabbit Polyclonal Antibody to ADAM22

    预测反应

    Rat,human - identical

    纯化方法

    Affinity purified on immobilized antigen.

    免疫原

    (C)HNDDAKTGITLSGNG, corresponding to amino acid residues 715-729 of mouse ADAM22

    亚型

    IgG
  • 应用备注

    WB: 1:200

    FC: The optimal concentration should be determined by the user

    ICC: The optimal concentration should be determined by the user

    IHC: 1:200

    IP: The optimal concentration should be determined by the user

    说明

    Negative Control: (ABIN7234619)

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    0.2 mL double distilled water (DDW)

    浓度

    1 mg/mL

    缓冲液

    PBS pH 7.4

    储存液

    Without preservative

    储存条件

    -20 °C

    储存方法

    The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20°C
  • 抗原

    ADAM22 (ADAM Metallopeptidase Domain 22 (ADAM22))

    别名

    Disintegrin and metalloproteinase domain-containing protein 22

    背景

    Synonyms: Disintegrin and metalloproteinase domain-containing protein 22, ADAM metallopeptidase domain 22, MDC2

    Description: ADAMs (a disintegrin and metalloproteinases) are multi-domain transmembrane glycoproteins with diverse roles in physiology and disease. Notably, 8 of 21 ADAMs lack functional metalloproteinase domains and are implicated in protein-protein interactions instead of membrane protein ectodomain shedding.ADAM22 is a non-proteinase which acts as a post synaptic receptor for the secreted neurotransmission modulator LGI-1 at neural synapses. ADAM22 is a compact four-leaf clover with the metalloproteinase-like domain (Domain M) held in the concave face of a rigid module formed by the disintegrin (Domain D), cysteine-rich (Domain C), and epidermal growth factor-like domains (Domain E). The largest domain in the four-leaf clover, domain M, is distal to the cell membrane. Following domain M, domain D and domain C zigzag to domain E in a compact, but not extended fashion. A 15-amino acid linker, leads the C terminus of domain E to the membrane. The loss of metalloproteinase activity is ensured by the absence of critical catalytic residues, the filling of the substrate groove, and the steric hindrance by the cysteine-rich domain. The extracellular domain of ADAM22 interacts with LGI-1, whereas its cytoplasmic PDZ-binding motif recruits PSD-95. The link of ADAM22 and LGI-1 to AMPA receptors establishes their roles in glutamate neurotransmission1.Mutations that impair LGI-1 binding to ADAM22 are implicated in the pathogenesis of Autosomal dominant lateral temporal epilepsy (ADTLE), a focal epilepsy syndrome characterized by focal seizures with prominent auditory or aphasic symptoms, normal magnetic resonance imaging, and usually benign evolution2.

    基因ID

    11496

    UniProt

    Q9R1V6
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