TSYL1 rabbit pAb
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT). [provided by RefSeq, Dec 2009],
Product Specifications
Background
The protein encoded by this gene is found in the nucleolus and is similar to that of a family of genes on the Y-chromosome. This gene is intronless. Defects in this gene are a cause of sudden infant death with dysgenesis of the testes syndrome (SIDDT) . [provided by RefSeq, Dec 2009]
UniProt
Q9H0U9
Swiss Prot
Q9H0U9
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human TSYL1 AA range: 211-261
Target
TSYL1
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, nucleolus .
Gene ID (Human)
7259
Available Sizes
Curated Selection
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