VMA21 Polyclonal Antibody
This is a VMA21 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.
Product Specifications
Background
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.
Synonyms
VMA21, Vacuolar ATPase Assembly Factor, Myopathy With Excessive Autophagy Protein, MEAX, XMEA, Vacuolar ATPase Assembly Integral Membrane Protein VMA21, VMA21 Vacuolar H+-ATPase Homolog (S. Cerevisiae), Myopathy With Excessive Autophagy, VMA21 Vacuolar H+-ATPase
Swiss Prot
Q3ZAQ7
Accession Number
NP001017980
Reactivity
Human, Mouse
Immunogen
Synthetic peptide of human VMA21
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Polyclonal Antibody
Applications
IHC, IF, ELISA
Purification Method
Antigen affinity purification
Assay Type
Antibody
Concentration
2.6 mg/mL
Dilution
IHC 1:150-1:500, IF 1: 50-1:200, ELISA 1:5000-1:240000
Buffer
PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Storage Conditions
Store at -20°C. Avoid freeze / thaw cycles.
Host or Source
Rabbit
Isotype
IgG
Available Sizes
Curated Selection
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