SAG anticorps (AA 193-405) (Biotin)
Aperçu rapide pour SAG anticorps (AA 193-405) (Biotin) (ABIN8034206)
Antigène
Voir toutes SAG AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 193-405
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Fonction
- Anti-Retinal S antigen/SAG Antibody Biotin Conjugated
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Specificité
- No cross reactivity with other proteins.
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Purification
- Immunogen affinity purified.
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Immunogène
- E. coli-derived human Retinal S antigen recombinant protein (Position: R193-E405).
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Isotype
- IgG
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Indications d'application
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- -20 °C
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Stockage commentaire
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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Date de péremption
- 12 months
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- SAG (S-Antigen, Retina and Pineal Gland (Arrestin) (SAG))
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Autre désignation
- SAG
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Sujet
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Background: S-arrestin is a protein that in humans is encoded by the SAG gene. Members of arrestin/beta-arrestin protein family are thought to participate in agonist-mediated desensitization of G-protein-coupled receptors and cause specific dampening of cellular responses to stimuli such as hormones, neurotransmitters, or sensory signals. 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 this gene have been associated with Oguchi disease, a rare autosomal recessive form of night blindness.
Gene Full Name: S-antigen visual arrestin
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ID gène
- 6295
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UniProt
- P10523
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Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling
Antigène
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