Human KIRREL3 ELISA Kit ELISA试剂盒,Human KIRREL3 ELISA Kit/人KIRREL3 ELISA试剂盒

2024-10-23

Human KIRREL3 ELISA Kit/人KIRREL3 ELISA试剂盒

货号:EH288RB,EH288RBX5,EH288RBX10

规格:96 tests,5X,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

0.21 ng/mL

检测范围0.21-50 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 nameKIRREL3
Protein aliasesKin of IRRE-like protein 3, Kin of irregular chiasm-like protein 3, nephrin-like 2, Nephrin-like protein 2, Processed kin of IRRE-like protein 3

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 aliasesKIAA1867, KIRRE, KIRREL3, MRD4, NEPH2, PRO4502, UNQ5923/PRO4502/PRO19814
Gene ID(Human) 84623
Gene symbolKIRREL3
UniProt ID(Human) Q8IZU9
Human KIRREL3 quantitates human KIRREL3 in serum, plasma, supernatant. The assay will exclusively recognize both natural and recombinant human KIRREL3.人KIRREL3定量检测血清,血浆,上清液中的人KIRREL3。 该检测试剂盒将专门识别天然和重组人KIRREL3。Target information 靶标信息The protein encoded by this gene is a member of the nephrin-like protein family. These proteins are expressed in fetal and adult brain, and also in podocytes of kidney glomeruli. The cytoplasmic domains of these proteins interact with the C-terminus of podocin, also expressed in the podocytes, cells involved in ensuring size- and charge-selective ultrafiltration. The protein encoded by this gene is a synaptic cell adhesion molecule with multiple extracellular immunoglobulin-like domains and a cytoplasmic PDZ domain-binding motif. Mutations in this gene are associated with several neurological and cognitive disorders. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.该基因编码的蛋白质是肾素样蛋白质家族的成员。 这些蛋白质在胎儿和成年大脑中以及肾小球的足细胞中表达。 这些蛋白质的胞质结构域与Podocin的C末端相互作用,Podocin的C末端也在足细胞中表达,足细胞是参与确保大小和电荷选择性超滤的细胞。 该基因编码的蛋白质是一个突触细胞粘附分子,具有多个细胞外免疫球蛋白样结构域和胞质PDZ结构域结合基序。 该基因的突变与几种神经和认知障碍有关。 已经发现该基因的编码不同同工型的剪接的转录变体。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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