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DROPARRAY

INSTRUMENTS FOR MULTIPLEX IMUNOASSAYS

DA-Bead 시스템과 플레이트를 사용한 소형화는 샘플 분량과 샘플과 비드의 소모를 1/5로 감소시키고
연구비용을 60% 이상까지 줄여줍니다. DropArray 세척방법은 효율적이며 비드의 응집을 제한합니다.

INSTRUMENTS FOR MULTIPLEX IMUNOASSAYS
  • Features
  • Technical specifications
  • Accessories and components
  • Scientific data

Features

LTMX

01

원심분리보다 우수한 데이터 품질 획득 및
뛰어난 세포 보전 가능

02

하나의 분석 키트당
5배 더 많은 샘플 실험 가능

03

기존 연구비용의 60~80%절약 가능

04

비드의 응집 감소

05

자동화 가능 * DropArray HT210만 해당

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Technical specifications

DropArray LT210
Washing Station MX
전압 요구 사항 전력 소비량 치수 무게
LT-210MX-01-01 100 - 240V 24V / 3.0A 38cm(15인치) x 25cm(10인치) x 33cm(13인치) 8kg(18lb)

Accessories and components

96 format LT magnet clamper 384 format LT magnet clamper
LT-CP-MAG-96-01 LT-CP-MAG-384-01

Scientific data

연구데이터
연구데이터

Giardia infection during protein deficiency and sufficiency influences cytokine production

Cytokine production by BMDCs in response to endotoxin is altered during giardiasis in a diet dependent manner.
Bone marrow cells were harvested from male C57BL/6 mice on a control (CD) or protein deficient diet (PD) that were challenged (CD/G, PD/G) or free of Giardia lamblia (CD, PD).
Cells were cultured in RPMI with 10% FBS, supplemented on days 0 and 3 with GM-CSF (10ng/mL; Peprotech), and harvested on day 6. 2.5x105 cells were plated
per well of a round bottom 96-well dish, and treated with cell culture media or LPS for 24h.
Cytokine levels in the supernatants were determined by ELISA (A, B) and Luminex (C, D).
For ELISA data, values in (A, B) represent fold change of cytokines after LPS treatment (1mcg/mL) compared to unstimulated media control.

= p<0.05 One-Way ANOVA with Tukey post-test.
For Luminex data, Cytokine values were normalized using fold-change relative to the mean value of the control group (C, D) for each cytokine and
then compared using One-Way ANOVA, Kruskal-Wallis and Tukey or Dunn’s post-test (D), p-value is as reported in D. A,B N = 6–12 mice, C,D n = 3–6 mice.