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Calreticulin 3 Protein (CALR3)

This Recombinant Calreticulin 3 protein is expressed in 大肠杆菌(E. Coli).
产品编号 ABIN7318227
发货至: 中国
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Quick Overview for Calreticulin 3 Protein (CALR3) (ABIN7318227)

抗原

See all Calreticulin 3 (CALR3) 蛋白
Calreticulin 3 (CALR3)

蛋白类型

Recombinant

宿主

  • 6
  • 2
  • 1
人

资源

  • 4
  • 3
  • 1
  • 1
大肠杆菌(E. Coli)

纯度

> 95 % as determined by reducing SDS-PAGE.
  • 原理

    Recombinant Human Calreticulin-3/CALR3 Protein

    序列

    Thr 20-Leu384

    产品特性

    Recombinant Human calreticulin-3 is produced by our E.coli expression system and the target gene encoding Thr20-Leu384 is expressed.

    过滤

    0.2 μm filtered

    内毒素水平

    < 1.0 EU per μg of the protein as determined by the LAL method.

    Biological Activity Comment

    Not validated for activity
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  • 限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    Lyophilized from a 0.2 μm filtered solution of 20 mM Tris-HCl, 150 mM NaCl, 5 % Trehalose, 5 % Mannitol, 0.02 % Tween 80, 1 mM EDTA, pH 8.0.
    Normally 5 % - 8 % trehalose, mannitol and 0.01 % Tween 80 are added as protectants before lyophilization.

    储存条件

    4 °C,-20 °C,-80 °C

    储存方法

    Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.

    有效期

    12 months
  • 抗原

    Calreticulin 3 (CALR3)

    别名

    Calreticulin-3/CALR3

    背景

    CALR3,CRT2,Calreticulin-3,calreticulin-2,calsperin,Calreticulin-3 belongs to the calreticulin family, members of which are calcium binding chaperones localized mainly in the endoplasmic reticulum. It can be divided into a N-terminal globular domain, a proline-rich P-domain forming an elongated arm-like structure and a C-terminal acidic domain. During spermatogenesis process, Calreticulin-3 may act as a lectin-independent chaperone for specific client proteins such as ADAM3. Defects in CALR3 are the cause of familial hypertrophic cardiomyopathy type 19 (CMH19), it is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain.

    分子量

    Calculated MW: 42.9 kDa

    Observed MW: 40-50 kDa

    基因ID

    125972

    UniProt

    Q96L12

    途径

    Activation of Innate immune Response
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