BUD31 antibody (AA 10-90)
Quick Overview for BUD31 antibody (AA 10-90) (ABIN7213868)
Target
See all BUD31 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 10-90
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Purpose
- BUD31 Polyclonal Antibody
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Specificity
- BUD31 Polyclonal Antibody detects endogenous levels of BUD31 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the N-terminal region of human BUD31 at AA range: 10-90
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), ELISA (1:20000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- BUD31 (BUD31 Homolog (BUD31))
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Alternative Name
- BUD31
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Background
- Rabbit Anti-BUD31 Polyclonal Antibody,BUD31, EDG2, Protein BUD31 homolog, Protein EDG-2, Protein G10 homolog,BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5 % of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.,Protein BUD31 homolog
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Molecular Weight
- observerd band 17kDa
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Gene ID
- 8896
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UniProt
- P41223
Target
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