MYL3/CMLC1 anticorps
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- Antigène Voir toutes MYL3/CMLC1 (MYL3) Anticorps
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp MYL3/CMLC1 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- Attributs du produit
- Polyclonal Antibody
- Purification
- Affinity purification
- Immunogène
- Recombinant protein of human MYL3
- Isotype
- IgG
- Top Product
- Discover our top product MYL3 Anticorps primaire
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- Indications d'application
- WB 1:1000-1:5000, IHC 1:50-1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.5 mg/mL
- Buffer
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
- Autre désignation
- MYL3 (MYL3 Produits)
- Synonymes
- anticorps CMD1S, anticorps CMH1, anticorps MPD1, anticorps MYHCB, anticorps SPMD, anticorps SPMM, anticorps B-MHC, anticorps MyHC-I, anticorps Myhc-b, anticorps Myhcb, anticorps beta-MHC, anticorps MLC1s, anticorps MLC1v, anticorps Mylc, anticorps VLC1, anticorps Mylc1v, anticorps CMH8, anticorps MLC1SB, anticorps MLC1V, anticorps mlc1v, anticorps myl3-a, anticorps myl3-b, anticorps myl3.L, anticorps zgc:103441, anticorps myosin heavy chain 7, anticorps myosin, heavy polypeptide 7, cardiac muscle, beta, anticorps myosin, light polypeptide 3, anticorps myosin light chain 3, anticorps myosin light chain 3 S homeolog, anticorps cardiac myosin light chain-1, anticorps MYH7, anticorps Myh7, anticorps Myl3, anticorps MYL3, anticorps myl3.S, anticorps cmlc1
- Sujet
- MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
- Poids moléculaire
- 22 kDa
- UniProt
- P08590
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