NCF1 Adenovirus (Human)

Product type

Adenovirus
Detection and sensitivity

Before using NCF1 Adenovirus (Human) please read the package insert. It is intended for Human reactivity. Accession Number: BC002816
Performance and applications

Please contact Gentaur's support by livechat, email or phone in order to receive the requested information. The product is for research use only.
Additional information

The NCF1 Adenovirus (Human) could be additionally purified if wanted from the customer. Please contact our sales representative to obtain more information.
Shipping handling and storage

NCF1 Adenovirus (Human) should be stored according to label on the vial.
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

NCF1 Adenovirus
Gene symbol

NCF1
Short name

NCF1 Adenovirus ( )
Species

Human, Humans
Alternative name

neutrophil cytosolic factor 1 Adenovirus (H. sapiens)
Alternative to gene target

neutrophil cytosolic factor 1, NCF1 and IDBG-21570 and ENSG00000158517 and 653361, phosphatidylinositol-3, Plasma membranes, Ncf1 and IDBG-202592 and ENSMUSG00000015950 and 17969, NCF1 and IDBG-639883 and ENSBTAG00000003305 and 281345
Virus

adenovirus

Identity

HGNC:7660
Gene

NCF1
Long gene name

neutrophil cytosolic factor 1
Synonyms gene name
- neutrophil cytosolic factor 1 (47kD, chronic granulomatous disease, autosomal 1)
Synonyms
- p47phox
- NOXO2
- NCF1A
- SH3PXD1A
Synonyms name
- NADPH oxidase organizer 2
- chronic granulomatous disease, autosomal 1
GenBank acession
- M25665
Locus

7q11.23
Discovery year

1989-05-25
Entrez gene record

653361
RefSeq identity
- NM_000265
VEGA ID

OTTHUMG00000149965
Locus Specific Databases
- NCF1base: Mutation registry for autosomal recessive chronic granulomatous disease (CGD), deficiency of p47phox
- LRG_87