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Antikörper

VMA21 Polyclonal Antibody

Produktgrößen
20 ul
£118,00
E-AB-53204-20UL
60 ul
£183,00
E-AB-53204-60UL
120 ul
£272,00
E-AB-53204-120UL
200 ul
£420,00
E-AB-53204-200UL
Über dieses Produkt
SKU:
E-AB-53204
Zusätzliche Namen:
Vacuolar ATPase Assembly Factor,MEAX,Myopathy With Excessive Autophagy,Myopathy With Excessive Autophagy Protein,VMA21,VMA21 Vacuolar H+-ATPase,VMA21 Vacuolar H+-ATPase Homolog (S. Cerevisiae),Vacuolar ATPase Assembly Integral Membrane Protein VMA21,XMEA
Anwendung:
Immunofluorescence, Immunohistochemistry
Buffer:
Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Klonalität:
Polyclonal
Konzentration:
2.6 mg/ml
Weitere Details:
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.
Host:
Rabbit
Immunogen:
Synthetic peptide of human VMA21
Isotyp:
IgG
Aufreinigung:
Affinity Purified
Reaktivitäten:
Human, Mouse
Versandbedingungen:
Blue Ice
Lagerbedingungen:
-20[o]C Avoid freeze/thaw cycles.
Hersteller:
Elabscience
Typ:
Antibody: Polyclonal Antibody