
Thermo Fisher Scientific ZNF408/PRDM17 (Transcription Factor) Monoclonal Antibody (PCRP-ZNF408-1E5)
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Applications
Tested Dilution
Publications
Western Blot (WB)
1-2 µg/mL
Flow Cytometry (Flow)
1-2 µg/10^6 cells
Peptide Array (Array)
Assay-dependent
Product Specifications
Species Reactivity
Human
Host/Isotype
Mouse / IgG2b
Class
Monoclonal
Type
Antibody
Clone
PCRP-ZNF408-1E5
Immunogen
Recombinant full-length human ZNF408 protein if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
ZNF408,
uniProtId:
Q9H9D4-1,
ncbiNodeId:
9606,
antigenRange:
1-720,
antigenLength:
720,
antigenImageFileName:
79797-MSM1-P0_ZNF408_Q9H9D4-1_House_mouse.svg,
antigenImageFileNamePDP:
79797-MSM1-P0_ZNF408_Q9H9D4-1_House_mouse_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
200 µg/mL
Purification
Protein A/G
Storage buffer
PBS, pH 7.4, with 0.05% BSA
Contains
0.05% sodium azide
Storage conditions
4° C
Shipping conditions
Ambient (domestic); Wet ice (international)
Target Information
Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Kruppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. As a member of the Kruppel C2H2-type zinc-finger protein family, ZNF396 (zinc finger protein 396), also known as PRDM17 (PR domain zinc finger protein 17), is a 720 amino acid nuclear protein that contains 10 C2H2-type zinc fingers. The gene encoding ZNF408 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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