ZNF592 rabbit pAb
Zinc finger protein 592 (ZNF592) Homo sapiens This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011],
Product Specifications
Background
Zinc finger protein 592 (ZNF592) Homo sapiens This gene is thought to play a role in a complex developmental pathway and the regulation of genes involved in cerebellar development. Mutations in this gene have been associated with autosomal recessive spinocerebellar ataxia. [provided by RefSeq, Jan 2011]
UniProt
Q92610
Swiss Prot
Q92610
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human ZNF592. AA range:961-1010
Clonality
Polyclonal
Source
Rabbit
Applications
WB; IHC; IF; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. Not yet tested in other applications.
Molecular Weight
160kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
160kD
Fragment
IgG
Subcellular Location
Nucleus .
Other Product Names
ZNF592; KIAA0211; Zinc finger protein 592
Gene ID (Human)
9640
Available Sizes
Curated Selection
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