VMA21 anticorps
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- Antigène Voir toutes VMA21 Anticorps
- VMA21 (Vacuolar H+-ATPase Homolog (VMA21))
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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 VMA21 est non-conjugé
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Application
- ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)
- Attributs du produit
- Polyclonal Antibody
- Purification
- Antigen affinity purification
- Immunogène
- Synthetic peptide of human VMA21
- Isotype
- IgG
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anti-Vacuolar H+-ATPase Homolog (VMA21) (N-Term) antibody
VMA21 Reactivité: Humain, Chien WB, IHC, IHC (p) Hôte: Lapin Polyclonal unconjugated
anti-Vacuolar H+-ATPase Homolog (VMA21) (N-Term) antibodyVMA21 Reactivité: Humain, Souris, Rat, Chien, Boeuf (Vache), Porc, Lapin WB, IHC Hôte: Lapin Polyclonal unconjugated
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- Indications d'application
- IHC 1:150-1:500, IF 1: 50-1:200, ELISA 1:5000-1:240000
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 2.6 mg/mL
- Buffer
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
- 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
- VMA21 (Vacuolar H+-ATPase Homolog (VMA21))
- Autre désignation
- VMA21 (VMA21 Produits)
- Synonymes
- anticorps MEAX, anticorps XMEA, anticorps ATP6H, anticorps ATP6V0E, anticorps M9.2, anticorps Vma21, anticorps Vma21p, anticorps RGD1566155, anticorps 2610030H06Rik, anticorps AI840175, anticorps VMA21, vacuolar ATPase assembly factor, anticorps ATPase H+ transporting V0 subunit e1, anticorps VMA21 vacuolar H+-ATPase homolog (S. cerevisiae), anticorps VMA21, vacuolar ATPase assembly factor L homeolog, anticorps VMA21, anticorps ATP6V0E1, anticorps Vma21, anticorps vma21.L
- Sujet
- This gene encodes a chaperone for assembly of lysosomal vacuolar ATPase. Required for the assembly of the V0 complex of the vacuolar ATPase (V-ATPase) in the endoplasmic reticulum. Associates with the V0 complex of the vacuolar ATPase (V-ATPase). MEAX is a childhood-onset disease characterized by progressive vacuolation and atrophy of skeletal muscle. It is inherited in recessive fashion, affecting boys and sparing carrier females. Onset is in childhood, and patients exhibit weakness of the proximal muscles of the lower extremities, progressing slowly to involve other skeletal muscle groups over time.
- UniProt
- Q3ZAQ7
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