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Merck
CN

RAB0110

Mouse CTLA-4 ELISA Kit

for serum, plasma and cell culture supernatant

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About This Item

NACRES:
NA.32
UNSPSC Code:
41116158
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Product Name

Mouse CTLA-4 ELISA Kit, for serum, plasma and cell culture supernatant

species reactivity

mouse

packaging

kit of 96 wells (12 strips x 8 wells)

technique(s)

ELISA: suitable
capture ELISA: suitable

input

sample type serum
sample type plasma
sample type cell culture supernatant(s)

assay range

inter-assay cv: <12%
intra-assay cv: <10%
sensitivity: 5 pg/mL
standard curve range: 4.92-1200 pg/mL

detection method

colorimetric

shipped in

wet ice

storage temp.

−20°C

Gene Information

mouse ... Ctla4(12477)

Application

For research use only. Not for use in diagnostic procedures.
Please refer to the attached General ELISA KIT Procedure (sandwich, competitive & Indirect ELISA)

General description

The Mouse CTLA4 (cytotoxic T-lymphocyte-associated molecule 4) ELISA (Enzyme-Linked Immunosorbent Assay) kit is an in vitro enzyme-linked immunosorbent assay for the quantitative measurement of mouse CTLA4 in serum, plasma, cell culture supernatants and urine.

Immunogen

Recombinant Mouse CTLA4

Other Notes

A sample Certificate of Analysis is available for this product.
Please type the word sample in the text box provided for lot number.

pictograms

Corrosion

signalword

Warning

hcodes

Hazard Classifications

Met. Corr. 1

Storage Class

8A - Combustible corrosive hazardous materials

Regulatory Information

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Monika Abramiuk et al.
Cells, 10(3) (2021-03-07)
Altered immune mechanisms are implicated in the pathogenesis of endometriosis. CTLA-4 is a membrane receptor that favors the anergic state of lymphocytes, which may disrupt the immune system response in the endometriotic environment. In this study, we examined the expression
Karel Balihar et al.
European journal of gastroenterology & hepatology, 26(8), 880-887 (2014-06-20)
Clostridium difficile infection (CDI) has been increasing in incidence, with significant morbidity and mortality, and is subject to geographical and institutional variability. We aimed to characterize epidemiology and clinical manifestations of CDI in a Czech tertiary care center and to
Amany Mansour et al.
Leukemia & lymphoma, 55(9), 2120-2124 (2013-11-29)
We herein evaluate the role of the B7-family molecule CD86 and the Cytotoxic T-lymphocyte-associated antigen-4 (CTLA-4) as a possible immunopathogenic factors in patients with ALL. The results of 60 patients with de novo ALL were compared to 40 controls. A

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