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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

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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