VMA21 Polyclonal Antibody | G-AB-06924

VMA21 Polyclonal Antibody | G-AB-06924 | Gentaur Antibodies

Overview: 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.

Category Type: Polyclonal Antibody

Research Areas: Cell Biology, Signal Transduction

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 Homolo.

Reactivity: Human, Mouse

Host: Rabbit

Isotype: IgG

Gene ID:

Accession #: NP001017980

Clonality: Polyclonal

Immunogen: Synthetic peptide of human VMA21

Clone #:

Conjugation: Unconjugated

Swissprot: Q3ZAQ7

Santa Cruz:

Calculated MW:

Observed MW:

Concentration: 2.6 mg/mL

Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4

Purification method: Antigen affinity purification

Application: IHC, IF, ELISA

Dilution: IHC 1:150-1:500, IF 1: 50-1:200, ELISA 1:5000-1:240000

Storage: Store at -20°C. Avoid freeze / thaw cycles.

VMA21 Polyclonal Antibody DataSheet