Thermo Fisher Scientific ZBTB20 Polyclonal Antibody

Applications

Tested Dilution

Publications

Immunohistochemistry (Paraffin) (IHC (P))

1:50-1:200

-

Immunocytochemistry (ICC/IF)

0.25-2 µg/mL

-

Product Specifications

Species Reactivity

Human

Host/Isotype

Rabbit / IgG

Class

Polyclonal

Type

Antibody

Immunogen

Recombinant protein corresponding to Human ZBTB20. Recombinant protein control fragment (Product #RP-91673). if (typeof window.$mangular === undefined || !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{targetFamily:ZBTB20,uniProtId:Q9HC78-1,ncbiNodeId:9606,antigenRange:389-538,antigenLength:741,antigenImageFileName:PA5-53496_ZBTB20_Q9HC78-1_Rabbit.svg,antigenImageFileNamePDP:PA5-53496_ZBTB20_Q9HC78-1_Rabbit_PDP.jpeg,sortOrder:1}\]; $mangular.isB2BCMGT = false; $mangular.isEpitopesModalImageMultiSizeEnabled = true;

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

Conjugate

Unconjugated Unconjugated Unconjugated

Form

Liquid

Concentration

0.05 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_2649761

Product Specific Information

Immunogen sequence: SVEQQFGPGA ARDSQAEPTQ PEQAAEAPAE GGPQTNQLET GASSPERSNE VEMDSTVITV SNSSDKSVLQ QPSVNTSIGQ PLPSTQLYLR QTETLTSNLR MPLTLTSNTQ VIGTAGNTYL PALFTTQPAG SGPKPFLFSL PQPLAGQQTQ

Highest antigen sequence identity to the following orthologs: Mouse - 91%, Rat - 90%.

Target Information

This gene, which was initially designated as dendritic cell-derived BTB/POZ zinc finger (DPZF), belongs to a family of transcription factors with an N-terminal BTB/POZ domain and a C-terminal DNA-bindng zinc finger domain. The BTB/POZ domain is a hydrophobic region of approximately 120 aa which mediates association with other BTB/POZ domain-containing proteins. This gene acts as a transcriptional repressor and plays a role in many processes including neurogenesis, glucose homeostasis, and postnatal growth. Mutations in this gene have been associated with Primrose syndrome as well as the 3q13.31 microdeletion syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Feb 2017]

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