Thermo Fisher Scientific FNBP4 Polyclonal Antibody

Applications

Tested Dilution

Publications

Western Blot (WB)

0.04-0.4 µg/mL

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Immunohistochemistry (IHC)

-

View 1 publication 1 publication

Immunohistochemistry (Paraffin) (IHC (P))

1:50-1:200

-

Immunocytochemistry (ICC/IF)

0.25-2 µg/mL

-

Product Specifications

Species Reactivity

Human

Published species

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant protein corresponding to Human FNBP4. Recombinant protein control fragment (Product #RP-97285). if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:FNBP4,uniProtId:Q8N3X1-1,ncbiNodeId:9606,antigenRange:482-567,antigenLength:1017,antigenImageFileName:PA5-59035_FNBP4_Q8N3X1-1_Rabbit.svg,antigenImageFileNamePDP:PA5-59035_FNBP4_Q8N3X1-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.1 mg/mL

Purification

Antigen affinity chromatography

Storage buffer

PBS, pH 7.2, with 40% glycerol

Contains

0.02% sodium azide

Storage conditions

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

Shipping conditions

Wet ice

RRID

AB_2641693

Product Specific Information

Immunogen sequence: NGETAIGAEN SEKIDENSDK EMEVEESPEK IKVQTTPKVE EEQDLKFQIG ELANTLTSKF EFLGINRQSI SNFHVLLLQT ETRIAD

Highest antigen sequence identity to the following orthologs: Mouse - 92%, Rat - 92%.

Target Information

FNBP4 encodes a protein containing two tryptophan-rich WW domains that binds the proline-rich formin homology 1 domains of formin family proteins, suggesting a role in the regulation of cytoskeletal dynamics during cell division and migration. It also binds intersectin family proteins suggesting a role in the maintenance of membrane curvature at sites of nascent vesicle formation. Naturally occurring mutations in this gene are associated with Waardenburg anophthalmia syndrome.

For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.