NSUN5P2 antibody
NSUN5P2
Reactivity: Human
WB, ELISA
Host: Rabbit
Polyclonal
unconjugated
1 image
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- Target See all NSUN5P2 products
- NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This NSUN5P2 antibody is un-conjugated
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Application
- Western Blotting (WB), ELISA
- Purification
- Antibody is purified by protein A chromatography method.
- Immunogen
- Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human NSUN5C.
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anti-NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2) (Middle Region) antibody
NSUN5P2 Reactivity: Human, Rabbit, Mouse, Rat, Cow, Dog, Guinea Pig, Horse WB Host: Rabbit Polyclonal unconjugated
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- Application Notes
- NSUN5C antibody can be used for detection of NSUN5C by ELISA at 1:312500. NSUN5C antibody can be used for detection of NSUN5C by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
- Concentration
- 1 mg/mL
- Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
- Handling Advice
- As with any antibody avoid repeat freeze-thaw cycles.
- Storage
- 4 °C/-20 °C
- Storage Comment
- For short periods of storage (days) store at 4 °C. For longer periods of storage, store NSUN5C antibody at -20 °C.
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- Target
- NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
- Alternative Name
- NSUN5C (NSUN5P2 Products)
- Synonyms
- NOL1R2 antibody, NSUN5C antibody, WBSCR20B antibody, WBSCR20C antibody, NOP2/Sun RNA methyltransferase family member 5 pseudogene 2 antibody, NSUN5P2 antibody
- Background
- NSUN5C gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder.This gene shares high sequence similarity with several genes in the Williams Beuren Syndrome critical region and its deletion is associated with this disorder. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.
- Molecular Weight
- 34 kDa
- Gene ID
- 260294
- NCBI Accession
- NP_115534
- UniProt
- Q63ZY6
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