SGCA anticorps (Middle Region)
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- Antigène Voir toutes SGCA Anticorps
- SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
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Épitope
- Middle Region
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp SGCA est non-conjugé
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Application
- Western Blotting (WB)
- Séquence
- QVIEVTAYNR DSFDTTRQRL VLEIGDPEGP LLPYQAEFLV RSHDAEEVLP
- Attributs du produit
- This is a rabbit polyclonal antibody against SGCA. It was validated on Western Blot.
- Purification
- Affinity purified
- Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of Human SGCA
- Top Product
- Discover our top product SGCA 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
- Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- Stock
- -20 °C
- Stockage commentaire
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- Antigène
- SGCA (Sarcoglycan, alpha (50kDa Dystrophin-Associated Glycoprotein) (SGCA))
- Autre désignation
- SGCA (SGCA Produits)
- Synonymes
- anticorps Sgca, anticorps 50-DAG, anticorps A2, anticorps ADL, anticorps DAG2, anticorps DMDA2, anticorps LGMD2D, anticorps SCARMD1, anticorps adhalin, anticorps 50DAG, anticorps Asg, anticorps sarcoglycan alpha, anticorps sarcoglycan, alpha (dystrophin-associated glycoprotein), anticorps sarcoglycan, alpha, anticorps SGCA, anticorps Sgca
- Sujet
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This gene encodes a component of the dystrophin-glycoprotein complex (DGC), which is critical to the stability of muscle fiber membranes and to the linking of the actin cytoskeleton to the extracellular matrix. Its expression is thought to be restricted to striated muscle. Mutations in this gene result in type 2D autosomal recessive limb-girdle muscular dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: SGCA, ADL, DAG2,
Protein Size: 263 - ID gène
- 6442
- NCBI Accession
- NP_001129169
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