Human Matriptase/ST14 ELISA Kit ELISA试剂盒,Human Matriptase/ST14 ELISA Kit/人Matriptase / ST14 ELISA试剂盒

2024-10-24

Human Matriptase/ST14 ELISA Kit/人Matriptase / ST14 ELISA试剂盒

货号:EH315RB,EH315RBX5,EH315RBX10

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

0.41 ng/mL

检测范围0.41-100 ng/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 nameST14
Protein aliasesMatriptase, Membrane-type serine protease 1, MT-SP1, Prostamin, Serine protease 14, Serine protease TADG-15, suppression of tumorigenicity 14 (colon carcinoma), suppression of tumorigenicity 14 (colon carcinoma, matriptase, epithin), Suppressor of tumorigenicity 14 protein, tumor associated differentially expressed gene 15 protein, Tumor-associated differentially-expressed gene 15 protein

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 aliasesARCI11, HAI, MT-SP1, MTSP1, PRSS14, SNC19, ST14, TADG15, TMPRSS14
Gene ID(Human) 6768
Gene symbolST14
UniProt ID(Human) Q9Y5Y6
Human Matriptase/ST14 quantitates human Matriptase/ST14 in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human Matriptase/ST14.人Matriptase / ST14定量检测血清,血浆,上清液中的人Matriptase / ST14。 该检测试剂盒将只识别天然和重组人Matriptase / ST14。Target information 靶标信息SOX2 is an intronless gene encoding a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The product of the SOX2 gene is required for stem-cell maintenance in the central nervous system, and also regulates gene expression in the stomach. The SOX2 gene lies within an intron of another gene called SOX2 overlapping transcript (SOX2OT). Further, SOX2 protein may act as a transcriptional activator after forming a protein complex with other proteins. Mutations in the SOX2 gene have been associated with bilateral anophthalmia, a severe form of structural eye malformation, optic nerve hypoplasia and syndromic microphthalmia.SOX2是一种无内含子基因,编码SRY相关HMG-box(SOX)转录因子家族的成员,参与调控胚胎发育和确定细胞命运。 SOX2基因的产物是中枢神经系统中干细胞维持所必需的,并且还调节胃中的基因表达。 SOX2基因位于另一个称为SOX2重叠转录本(SOX2OT)的基因的内含子内。 此外,在与其他蛋白质形成蛋白质复合物之后,SOX2蛋白质可以充当转录激活因子。 SOX2基因的突变与双侧性眼炎,结构性眼畸形,视神经发育不全和综合性小眼症的严重形式有关。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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