Human Tripeptidyl-peptidase I/TPP1 ELISA Kit ELISA试剂盒,Human Tripeptidyl-peptidase I/TPP1 ELISA Kit/人三肽基肽酶I / TPP1 ELISA试剂盒

2024-10-24

Human Tripeptidyl-peptidase I/TPP1 ELISA Kit/人三肽基肽酶I / TPP1 ELISA试剂盒

货号:EH465RB,EH465RBX5,EH465RBX10

规格:96 Tests,5X96 Tests,10X96 tests

价格:6641,29884,57271

产品类型:Platinum ELISA

品牌:Thermo Fisher

物种:人

宿主:其它

抗体亚型:其它

荧光染料:其它

灵敏度

10 pg/mL

检测范围10-2,500 pg/mL

样本类型/体积

血清 50 μL

血浆 50 μL

上清液 50 μL

操作时间

1 hr 20 min

测试时间

4 hr 45 min

Homogenous (no wash)

No

批间变异系数(CV)<12%
批内变异系数(CV)<10%

仪器设备

Colorimetric Microplate Reader 酶标仪

规格

5 x 96 Tests

组份

- 预包被96孔板

- 标准品

- 测定稀释浓缩液

- 生物素化检测抗体

- SAV-HRP

- 洗涤液

- 显色剂

- 终止液

- 胶板盖

储存温度

2-8℃

Protein nameCLN2
Protein aliasesCell growth-inhibiting gene 1 protein, growth-inhibiting protein 1, LPIC, lysosomal pepstatin insensitive protease, Lysosomal pepstatin-insensitive protease, TPP-1, TPP-I, Tripeptidyl aminopeptidase, tripeptidyl peptidase I, Tripeptidyl-peptidase 1, Tripeptidyl-peptidase I

物种(Tested)

试剂盒类型

Sandwich ELISA Kit

标记(染料)

HRP

检测抗体偶联物Biotin
Gene aliasesCLN2, GIG1, LPIC, SCAR7, TPP-1, TPP1, UNQ267/PRO304
Gene ID(Human) 1200
Gene symbolTPP1
UniProt ID(Human) O14773
Human Tripeptidyl-peptidase I/TPP1 quantitates human Tripeptidyl-peptidase I/TPP1 in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human Tripeptidyl-peptidase I/TPP1.人三肽基肽酶I / TPP1定量检测血清,血浆,上清液中的人三肽基肽酶I / TPP1。 该检测试剂盒将专门识别天然和重组人三肽基肽酶I / TPP1。Target information 靶标信息This gene encodes a member of the sedolisin family of serine proteases. The protease functions in the lysosome to cleave N-terminal tripeptides from substrates, and has weaker endopeptidase activity. It is synthesized as a catalytically-inactive enzyme which is activated and auto-proteolyzed upon acidification. Mutations in this gene result in late-infantile neuronal ceroid lipofuscinosis, which is associated with the failure to degrade specific neuropeptides and a subunit of ATP synthase in the lysosome.该基因编码丝氨酸蛋白酶的sedolisin家族的成员。 蛋白酶在溶酶体中发挥功能,可从底物上裂解N端三肽,并具有较弱的内肽酶活性。 它被合成为一种无催化活性的酶,该酶在酸化后会被激活并进行蛋白水解。 该基因的突变导致婴儿后期神经元类脂褐质病,这与降解特定的神经肽和溶酶体中的ATP合酶亚基失败有关。For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.仅供研究使用。 不用于诊断过程。 未经明确授权不得转售。

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