Human ICOS CRISPR Knock Out A549 Cell Line

Cell line type

A549
NCBI number

NM_012092
Availability

Please contact us every day to check the availability and/or to request a quote. For larger or bulk quantities a discount may apply.
Ordering

If you wish to order this product, please include the catalogue number #K1011453in your purchase order among with your shipping and billing information.
Technical file

Please contact us to request the latest datasheet, protocol, certificate of analysis and SDS files.
Notes

Designed for Research Use Only. Manufactured in Canada.
Other products
Description

For cells, cell lines and tissues in culture till half confluency.
Properties

Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.

Gene target

ICOS CRISPR Knock Out A549 Line
Gene symbol

ICOS, ICOSLG
Short name

ICOS CRISPR Knock Out A549 Line
Species

Human, Humans
Alternative name

H. sapiens inducible T-cell co-stimulator CRISPR Knock Out A549 cellular Line
Alternative to gene target

inducible T-cell co-stimulator, ICOS and IDBG-79246 and ENSG00000163600 and 29851, protein binding, Extracellular, Icos and IDBG-159737 and ENSMUSG00000026009 and 54167, ICOS and IDBG-643378 and ENSBTAG00000021596 and 507026
Tissue

cell

Identity

HGNC:5351
Gene

ICOS
Long gene name

inducible T cell costimulator
Synonyms gene name
- inducible T-cell costimulator
Synonyms
- AILIM
- CD278
Synonyms name
- activation-inducible lymphocyte immunomediatory molecule
GenBank acession
- AB023135
Locus

2q33.2
Discovery year

2000-02-29
Entrez gene record

29851
Pubmed identfication
- 9930702
- 10617205
RefSeq identity
- NM_012092
Classification
- CD molecules
VEGA ID

OTTHUMG00000132880
Locus Specific Databases
- ICOSbase: Mutation registry for ICOS deficiency
- LRG_65