1. Membrane Transporter/Ion Channel Neuronal Signaling
  2. iGluR
  3. Pep2-AVKI

Pep2-AVKI 是 AMPA 受体亚基 (GluR2) 亚基 (位于 C 末端 PDZ 位点) 与 C 激酶 (PICK1) 结合的选择性肽抑制剂。Pep2-AVKI 不影响 (AMPA 型谷氨酸受体) GluA2 与 GRIP 或 ABP 的结合。Pep2-AVKI 不增加 AMPA 电流幅度。Pep2-AVKI 可用于神经系统疾病的研究。

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Custom Peptide Synthesis

Pep2-AVKI

Pep2-AVKI Chemical Structure

CAS No. : 1315378-69-8

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  • 生物活性

  • 纯度 & 产品资料

  • 参考文献

生物活性

Pep2-AVKI is a selective peptide inhibitor of the binding of the AMPA receptor subunit (GluR2) at the C-terminal PDZ site to C-kinase (PICK1). Pep2-AVKI does not affect the binding of (AMPA-type glutamate receptor) GluA2 to GRIP or ABP. Pep2-AVKI does not increase the amplitude of AMPA currents. pep2-AVKI can be used to study neurological diseases[1][2][3][4].

体外研究
(In Vitro)

Pep2-AVKI (1 mM) 在小脑星状细胞中选择性地与 PICK 结合,不会改变 (微型兴奋性突触后电流) mEPSC 振幅或频率,但抑制了活性诱导的 (兴奋性突触后电流) EPSC 振幅比的增加[1]

Pep2-AVKI (1 mM) 在小脑星状细胞中阻断了含有突触 GluR2 的受体增加[1]

Pep2-AVKI 在海马突触体中增加了 AMPA 诱发的 (放射性标记的去甲肾上腺素) [3H]NA 和 (放射性标记的 D-天冬氨酸) [3H]D-ASP,增加 10 μM NMDA/1 μM 甘氨酸/50 μM (S) AMPA 诱导的氚释放,但不会改变 10 μM NMDA/1 μM 甘氨酸诱导的 [3H]D-ASP 释放[2][3]

Pep2-AVKI (100 μM) 在突触后神经元中阻断了 (长时程抑制) LTD[4]

MCE has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

1268.46

Formula

C60H93N13O17

CAS 号
Sequence

Tyr-Asn-Val-Tyr-Gly-Ile-Glu-Ala-Val-Lys-Ile

Sequence Shortening

YNVYGIEAVKI

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Please store the product under the recommended conditions in the Certificate of Analysis.

纯度 & 产品资料
参考文献
  • 摩尔计算器

  • 稀释计算器

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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Pep2-AVKI
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HY-P1059
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