2002
DOI: 10.1016/s0145-2126(01)00115-1
|View full text |Cite
|
Sign up to set email alerts
|

CD56+, NKp46+ cell line (MZ93) expressing T-cell and myeloid antigens

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2002
2002
2015
2015

Publication Types

Select...
4

Relationship

0
4

Authors

Journals

citations
Cited by 4 publications
(1 citation statement)
references
References 34 publications
0
1
0
Order By: Relevance
“…One microgram RNA was used for cDNA synthesis. Human NKp46 was amplified using the primers 5′‐CCGAATTAAACCTGTATCAAGA‐3′ and 5′‐AACTTCCCAACATCCTCCT‐3′ . cDNA synthesis and PCR amplification were performed on a TaKaRa PCR Thermal Cycler Dice Standard (TaKaRa, Kyoto, Japan) using the following thermal protocol: 50°C for 30 min and 95°C for 2 min, followed by 40 cycles of 95°C for 1 min, 60°C for 1 min, and 72°C for 1 min and a final extension step for 10 min at 72°C.…”
Section: Methodsmentioning
confidence: 99%
“…One microgram RNA was used for cDNA synthesis. Human NKp46 was amplified using the primers 5′‐CCGAATTAAACCTGTATCAAGA‐3′ and 5′‐AACTTCCCAACATCCTCCT‐3′ . cDNA synthesis and PCR amplification were performed on a TaKaRa PCR Thermal Cycler Dice Standard (TaKaRa, Kyoto, Japan) using the following thermal protocol: 50°C for 30 min and 95°C for 2 min, followed by 40 cycles of 95°C for 1 min, 60°C for 1 min, and 72°C for 1 min and a final extension step for 10 min at 72°C.…”
Section: Methodsmentioning
confidence: 99%