GLIS2 rabbit pAb
This gene is a member of the GLI-similar Zinc finger protein family and encodes a nuclear transcription factor with five C2H2-type zinc finger domains. The protein encoded by this gene is widely expressed at low levels in the neural tube and peripheral nervous system and likely promotes neuronal differentiation. It is abundantly expressed in the kidney and may have a role in the regulation of kidney morphogenesis. p120 regulates the expression level of this protein and induces the cleavage of this protein's C-terminal zinc finger domain. This protein also promotes the nuclear translocation of p120. Mutations in this gene cause nephronophthisis (NPHP), an autosomal recessive kidney disease characterized by tubular basement membrane disruption, interstitial lymphohistiocytic cell infiltration, and development of cysts at the corticomedullary border of the kidneys. [provided by RefSeq, Jan 2010],
Product Specifications
Background
UniProt
Q9BZE0
Swiss Prot
Q9BZE0
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human GLIS2 AA range: 442-492
Target
GLIS2
Clonality
Polyclonal
Source
Rabbit
Applications
WB
Concentration
1 mg/ml
Dilution
WB 1:500-2000
Buffer
-20°C/1 year
Storage Conditions
-20°C/1 year
Fragment
IgG
Subcellular Location
Nucleus speckle . Cytoplasm .
Gene ID (Human)
84662
Available Sizes
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