SAG antibody (AA 210-290)
Quick Overview for SAG antibody (AA 210-290) (ABIN7227368)
Target
See all SAG AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 210-290
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Purpose
- ARRS Polyclonal Antibody
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Specificity
- The antibody detects endogenous levels of ARRS 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 ARRS protein at AA range: 210-290
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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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- SAG (S-Antigen, Retina and Pineal Gland (Arrestin) (SAG))
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Alternative Name
- ARRS
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Background
- Rabbit Anti-ARRS Polyclonal Antibody,S-arrestin, 48 kDa protein, Retinal S-antigen, Rod photoreceptor arrestin,SAG (S-Antigen Visual Arrestin) is a Protein Coding gene. Diseases associated with SAG include Oguchi Disease-1 and Retinitis Pigmentosa 47. Among its related pathways are Phototransduction and Visual Cycle in Retinal Rods. S-arrestin, also known as S-antigen, is a major soluble photoreceptor protein that is involved in desensitization of the photoactivated transduction cascade. It is expressed in the retina and the pineal gland and inhibits coupling of rhodopsin to transducin in vitro. Additionally, S-arrestin is highly antigenic, and is capable of inducing experimental autoimmune uveoretinitis. Mutations in SAG have been associated with Oguchi disease, a rare autosomal recessive form of night blindness.,ARRS
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Gene ID
- 6295
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UniProt
- P10523
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Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling
Target
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