Retinal S antigen (SAG) Mouse Monoclonal Antibody (Biotin conjugated) [Clone ID: OTI7A12]

CAT#: TA812590AM

SAG mouse monoclonal antibody,clone OTI7A12, Biotinylated

Product Images

HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY SAG (RC220057, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-SAG (1:500). Positive lysates LY424652 (100ug) and LC424652 (20ug) can be purchased separately from OriGene.

Specifications

Product Data

• Clone Name: OTI7A12
• Applications: WB
• Recommended Dilution: WB 1:500
• Reactivities: Human, Mouse, Rat
• Host: Mouse
• Isotype: IgG1
• Clonality: Monoclonal
• Immunogen: Full length human recombinant protein of human SAG (NP_000532) produced in HEK293T cell.
• Formulation: PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
• Concentration: 0.5 mg/ml
• Purification: Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
• Conjugation: Biotin
• Storage: Store at -20°C as received.
• Stability: Stable for 12 months from date of receipt.
• Predicted Protein Size: 44.9 kDa
• Gene Name: S-antigen; retina and pineal gland (arrestin)
• Database Link:
  NP_000532
  Entrez Gene 20215 MouseEntrez Gene 25539 RatEntrez Gene 6295 Human
  UniProt ID P10523
• Background: 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. [provided by RefSeq, Jul 2008]
• Synonyms: RP47; S-AG

Reference Data

• Protein Families: Druggable Genome