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RYR1 antibody

RYR1 Reactivity: Human, Mouse, Rat ELISA, WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7003086
  • Target See all RYR1 Antibodies
    RYR1 (Ryanodine Receptor 1 (Skeletal) (RYR1))
    Reactivity
    • 22
    • 10
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 20
    • 2
    Rabbit
    Clonality
    • 21
    • 2
    Polyclonal
    Conjugate
    • 10
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This RYR1 antibody is un-conjugated
    Application
    • 11
    • 8
    • 6
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    ELISA, Western Blotting (WB)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Synthetic peptide of human RYR1
    Isotype
    IgG
    Top Product
    Discover our top product RYR1 Primary Antibody
  • Application Notes
    WB 1:200-1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.3 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    RYR1 (Ryanodine Receptor 1 (Skeletal) (RYR1))
    Alternative Name
    RYR1 (RYR1 Products)
    Synonyms
    ryr1 antibody, RYR1 antibody, alphaRYR antibody, CCO antibody, MHS antibody, MHS1 antibody, RYDR antibody, RYR antibody, RYR-1 antibody, SKRR antibody, Ryr1l antibody, CRC antibody, AI528790 antibody, Ryr antibody, skrr antibody, ryanodine receptor 1 antibody, ryanodine receptor 1 (skeletal) antibody, ryanodine receptor 1a (skeletal) antibody, ryanodine receptor 1, skeletal muscle antibody, RYR1 antibody, ryr1a antibody, Ryr1 antibody
    Background
    This gene encodes a ryanodine receptor found in skeletal muscle. The encoded protein functions as a calcium release channel in the sarcoplasmic reticulum but also serves to connect the sarcoplasmic reticulum and transverse tubule. Mutations in this gene are associated with malignant hyperthermia susceptibility, central core disease, and minicore myopathy with external ophthalmoplegia. Alternatively spliced transcripts encoding different isoforms have been described.
    Molecular Weight
    565 kDa
    NCBI Accession
    NP_000531
    UniProt
    P21817
    Pathways
    Myometrial Relaxation and Contraction, Skeletal Muscle Fiber Development
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