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Glucosylceramidase antibody (N-Term)

This Rabbit Polyclonal antibody specifically detects Glucosylceramidase in WB. It exhibits reactivity toward Human, Mouse, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit and Rat.
Catalog No. ABIN5514399
$483.54
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Quick Overview for Glucosylceramidase antibody (N-Term) (ABIN5514399)

Target

Glucosylceramidase (GLCM)

Reactivity

Human, Mouse, Cow, Dog, Guinea Pig, Horse, Pig, Rabbit, Rat

Host

  • 5
  • 1
Rabbit

Clonality

  • 5
  • 1
Polyclonal

Conjugate

  • 4
  • 1
  • 1
This Glucosylceramidase antibody is un-conjugated

Application

  • 6
  • 3
  • 3
  • 3
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 4
    • 4
    N-Term

    Sequence

    FSSPSREECP KPLSRVSIMA GSLTGLLLLQ AVSWASGARP CIPKSFGYSS

    Predicted Reactivity

    Cow: 75%, Dog: 75%, Guinea Pig: 75%, Horse: 75%, Human: 100%, Mouse: 75%, Pig: 79%, Rabbit: 75%, Rat: 75%

    Characteristics

    This is a rabbit polyclonal antibody against GLCM. It was validated on Western Blot.

    Purification

    Affinity purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N-terminal region of Human GLCM
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

    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

    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target

    Glucosylceramidase (GLCM)

    Alternative Name

    GLCM

    Background

    This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants.

    Alias Symbols: GBA, GC, GLUC,

    Protein Interaction Partner: NUDCD1, UBC, ITCH, ATP6V1B1, SNCA, FBXO6, TCP1, CBL, NEDD4, PARK2, HSP90AA1, HSPA4, PSAP,

    Protein Size: 536

    Gene ID

    2629

    NCBI Accession

    XP_006711333

    UniProt

    P04062
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