RNASET2 Protein (His tag)
Quick Overview for RNASET2 Protein (His tag) (ABIN7197719)
Target
See all RNASET2 ProteinsProtein Type
Origin
Source
Purity
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Purification tag / Conjugate
- This RNASET2 protein is labelled with His tag.
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Purpose
- Recombinant Human RNASET2 Protein (Baculovirus, His Tag)
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Sequence
- Met 1-His 256
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Characteristics
- A DNA sequence encoding the human RNASET2 isoform 1 (O00584-1) (Met 1-His 256) was fused with a polyhistidine tag at the C-terminus.
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Endotoxin Level
- < 1.0 EU per μg as determined by the LAL method.
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Ribonuclease T2 (RNASET2) (AA 172-256) protein (His-IF2DI Tag)
RNASET2 Origin: Human Host: Escherichia coli (E. coli) Recombinant Greater than 90 % as determined by SDS-PAGE. WB, ELISA
Ribonuclease T2 (RNASET2) (AA 1-256) protein (GST tag)RNASET2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AP, AA
Ribonuclease T2 (RNASET2) protein (Myc-DYKDDDDK Tag)RNASET2 Origin: Human Host: HEK-293 Cells Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Please refer to the printed manual for detailed information.
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Buffer
- Lyophilized from sterile 20 mM Tris, 500 mM NaCl, pH 7.4, 10 % glycerol
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Storage
- 4 °C,-20 °C,-80 °C
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Storage Comment
- Generally, lyophilized proteins are stable for up to 12 months when stored at -20 to -80°C. Reconstituted protein solution can be stored at 4-8°C for 2-7 days. Aliquots of reconstituted samples are stable at < -20°C for 3 months.
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- RNASET2 (Ribonuclease T2 (RNASET2))
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Alternative Name
- RNASET2
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Background
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Background: RNASET2 (ribonuclease T2) is an enzyme which belongs to the RNase T2 family. It is highly expressed in the temporal lobe and fetal brain. RNASET2 gene is a novel member of the Rh/T2/S-glycoprotein class of extracellular ribonucleases. It is a single copy gene that maps to 6q27, a region associated with human malignancies and chromosomal rearrangement. Defects in RNASET2 are the cause of leukoencephalopathy cystic without megalencephaly. An infantile-onset syndrome of cerebral leukoencephalopathy. Affected newborns develop microcephaly and neurologic abnormalities including psychomotor impairment, seizures and sensorineural hearing impairment. The brain shows multifocal white matter lesions, anterior temporal lobe subcortical cysts, pericystic abnormal myelination, ventriculomegaly and intracranial calcifications.
Synonym: Ribonuclease T2,3.1.27.-,Ribonuclease 6,RNASE6PL
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Molecular Weight
- 28.5 kDa
Target
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