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ZFP64 Recombinant antibody, PBS Only

ZFP64 Uni-rAbTM Recombinant Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

Conjugate

Unconjugated

CloneNo.

240847F9

Cat no : 83825-3-PBS

Synonyms

ZNF338, Zinc finger protein 64, Zfp-64, Zfp 64, 240847F9

Validation Data Gallery

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  • Western Blot (WB) analysis of various lysates using ZFP64 Recombinant antibody (83825-3-RR)

    WB analysis using 83825-3-RR (same clone as 83825-3-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 83825-3-RR (ZFP64 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 83825-3-PBS in a different storage buffer formulation.

  • Affinity and Kinetic Characterization of 83825-3-RR

    Affinity and Kinetic Characterization of 83825-3-RR

    Biolayer interferometry (BLl) kinetic assays of 83825-3-RR against Human ZFP64 were performed. The affinity constant is 1.53 nM.

Product Information

The immunogen of 83825-3-PBS is ZFP64 Fusion Protein expressed in E. coli.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen ZFP64 fusion protein Ag10971
Full Name zinc finger protein 64 homolog (mouse)
Calculated Molecular Weight 681 aa, 75 kDa
Observed Molecular Weight 70 kDa
GenBank Accession NumberBC041622
Gene Symbol ZFP64
Gene ID (NCBI) 55734
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

ZFP64 (also known as ZNF338) is a member of the Krüppel C2H2-type zinc finger family. ZFP64 is a coactivator of Notch1, mediating mesenchymal cell differentiation. ZFP64 expression was up-regulated in mouse peritoneal macrophages in response to stimulation with the TLR4 ligand LPS with a 2-fold increase. The MLL gene encoding the MLL fusion protein is easily activated by ZFP64. ZFP64 is essential for the continuous production of MLL fusion proteins in blood cancer and produces more cancer cells. Since ZFP64 deletion completely and specifically inhibits MLL fusion protein production and leukemia cascade growth, it is an ideal drug target.