NSUN5P2 antibody
The Rabbit Polyclonal anti-NSUN5P2 antibody is suitable to detect NSUN5P2 in samples from Human. It has been validated for WB and ELISA.
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Catalog No. ABIN2463242
$650.38
Plus shipping costs $50.00
100 μL
Shipping to:
United States
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Quick Overview for NSUN5P2 antibody (ABIN2463242)
Target
NSUN5P2
(NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
Reactivity
Human
Host
Rabbit
Clonality
Polyclonal
Conjugate
This NSUN5P2 antibody is un-conjugated
Application
Western Blotting (WB), ELISA
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Purification
- Antibody is purified by protein A chromatography method.
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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 WB Host: Rabbit Polyclonal unconjugated
anti-NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2) (Middle Region) antibodyNSUN5P2 Reactivity: Human, Rabbit, Cow, Dog, Guinea Pig, Horse, Mouse, Rat 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.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 100 ?L of distilled water. Final antibody concentration is 1 mg/mL.
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Concentration
- 1 mg/mL
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Buffer
- Antibody is lyophilized in PBS buffer with 2 % sucrose.
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Handling Advice
- As with any antibody avoid repeat freeze-thaw cycles.
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Storage
- 4 °C/-20 °C
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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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- NSUN5P2 (NOP2/Sun Domain Family, Member 5 Pseudogene 2 (NSUN5P2))
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Alternative Name
- NSUN5C
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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.
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Molecular Weight
- 34 kDa
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Gene ID
- 260294
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NCBI Accession
- NP_115534
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UniProt
- Q63ZY6
Target
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