GLRB anticorps (N-Term)
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- Antigène Voir toutes GLRB Anticorps
- GLRB (Glycine Receptor, beta (GLRB))
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Épitope
- AA 102-132, N-Term
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Reactivité
- Humain, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp GLRB est non-conjugé
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Application
- Western Blotting (WB), Enzyme Immunoassay (EIA)
- Specificité
- This antibody recognizes Human and Mouse Glycine receptor beta (N-term).
- Purification
- Protein A column, followed by peptide affinity purification
- Immunogène
- KLH conjugated synthetic peptide between 102-132 amino acids from the N-terminal region of Human Glycine receptor beta Genename: GLRB
- Isotype
- Ig Fraction
- Top Product
- Discover our top product GLRB Anticorps primaire
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- Indications d'application
- Optimal working dilution should be determined by the investigator.
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.25 mg/mL
- Buffer
- PBS containing 0.09 % (W/V) Sodium Azide as preservative
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Conseil sur la manipulation
- Avoid repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Antigène
- GLRB (Glycine Receptor, beta (GLRB))
- Autre désignation
- Glycine Receptor beta (GLRB Produits)
- Sujet
- This gene encodes the beta subunit of the glycine receptor, which is a pentamer composed of alpha and beta subunits. The receptor functions as a neurotransmitter-gated ion channel, which produces hyperpolarization via increased chloride conductance due to the binding of glycine to the receptor. Mutations in this gene cause startle disease, also known as hereditary hyperekplexia or congenital stiff-person syndrome, a disease characterized by muscular rigidity. Alternative splicing results in multiple transcript variants.Synonyms: GLRB, Glycine receptor 58 kDa subunit
- Poids moléculaire
- 56122 Da
- ID gène
- 2743
- NCBI Accession
- NP_000815
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