Glycogen Synthase 1 antibody (AA 60-640)
Quick Overview for Glycogen Synthase 1 antibody (AA 60-640) (ABIN7602155)
Target
See all Glycogen Synthase 1 (GYS1) AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 60-640
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Purpose
- Anti-Glycogen synthase 1/GYS1 Antibody
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Cross-Reactivity (Details)
- No cross-reactivity with other proteins.
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Characteristics
- Anti-Glycogen synthase 1/GYS1 Antibody (ABIN7602155). Tested in ELISA, Flow Cytometry, IF, IHC, ICC, WB applications. This antibody reacts with Human, Mouse, Rat. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogen
- E.coli-derived human Glycogen synthase 1/GYS1 recombinant protein (Position: D60-A640).
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Isotype
- IgG
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Application Notes
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Western blot, 0.1-0.25 μg/mL, Mouse, Rat
Immunohistochemistry(Paraffin-embedded Section), 2-5 μg/mL, Human, Mouse
Immunocytochemistry/Immunofluorescence, 5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x106 cells, Human
ELISA, 0.1-0.5 μg/mL, -
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.
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Storage
- 4 °C,-20 °C
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Storage Comment
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At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
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- Glycogen Synthase 1 (GYS1) (Glycogen Synthase 1 (Muscle) (GYS1))
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Alternative Name
- GYS1
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Background
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Synonyms: Rhombotin-2, Cysteine-rich protein TTG-2, LIM domain only protein 2, LMO-2, T-cell translocation protein 2, LMO2, RBTN2, RBTNL1, RHOM2, TTG2
Background: Glycogen synthase (UDP-glucose-glycogen glucosyltransferase) is a key enzyme in glycogenesis, the conversion of glucose into glycogen. The protein encoded by this gene catalyzes the addition of glucose monomers to the growing glycogen molecule through the formation of alpha-1,4-glycoside linkages. Mutations in this gene are associated with muscle glycogen storage disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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Molecular Weight
- 84-90 kDa
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Gene ID
- 2997
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UniProt
- P13807
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Pathways
- PI3K-Akt Signaling, AMPK Signaling, Cellular Glucan Metabolic Process
Target
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