TPGS2 antibody
Quick Overview for TPGS2 antibody (ABIN7230614)
Target
See all TPGS2 (C18orf10) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Purpose
- PGS2 Polyclonal Antibody
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Specificity
- The antibody detects endogenous levels of PGS2 protein
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Purification
- The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen
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Immunogen
- Synthesized peptide derived from part region of human PGS2 protein
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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), ELISA (1:5000-1:20000).
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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, pH 7.4, containing 0.02 % Sodium Azide as preservative and 50 % Glycerol.
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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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- TPGS2 (C18orf10) (Chromosome 18 Open Reading Frame 10 (C18orf10))
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Alternative Name
- PGS2
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Background
- Rabbit Anti-PGS2 Polyclonal Antibody,Decorin, Bone proteoglycan II, PG-S2, PG40,DCN encodes a member of the small leucine-rich proteoglycan family of proteins. Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed to generate the mature protein. Decorin plays a role in collagen fibril assembly. Binding of this protein to multiple cell surface receptors mediates its role in tumor suppression, including a stimulatory effect on autophagy and inflammation and an inhibitory effect on angiogenesis and tumorigenesis. This gene and the related gene biglycan are thought to be the result of a gene duplication. Mutations in this gene are associated with congenital stromal corneal dystrophy in human patients.,PGS2
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Molecular Weight
- observerd band 39kDa
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Gene ID
- 1634
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UniProt
- P07585
Target
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