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GBA antibody (AA 40-250)

This anti-GBA antibody is a Rabbit Polyclonal antibody detecting GBA in WB. Suitable for Human.
Catalog No. ABIN6140986

Quick Overview for GBA antibody (AA 40-250) (ABIN6140986)

Target

See all GBA Antibodies
GBA (Glucosidase, Beta, Acid (GBA))

Reactivity

  • 75
  • 46
  • 34
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 92
  • 12
Rabbit

Clonality

  • 84
  • 20
Polyclonal

Conjugate

  • 45
  • 20
  • 12
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GBA antibody is un-conjugated

Application

  • 73
  • 41
  • 26
  • 24
  • 13
  • 11
  • 11
  • 9
  • 5
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 7
    • 6
    • 5
    • 5
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    AA 40-250

    Sequence

    ARPCIPKSFG YSSVVCVCNA TYCDSFDPPT FPALGTFSRY ESTRSGRRME LSMGPIQANH TGTGLLLTLQ PEQKFQKVKG FGGAMTDAAA LNILALSPPA QNLLLKSYFS EEGIGYNIIR VPMASCDFSI RTYTYADTPD DFQLHNFSLP EEDTKLKIPL IHRALQLAQR PVSLLASPWT SPTWLKTNGA VNGKGSLKGQ PGDIYHQTWA R

    Cross-Reactivity

    Human

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 40-250 of human Glucosylceramidase beta (Glucosylceramidase beta (GBA)) (NP_000148.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Comment

    HIGH QUALITY

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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

    GBA (Glucosidase, Beta, Acid (GBA))

    Alternative Name

    GBA

    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.,GBA,GBA1,GCB,GLUC,Cancer,Signal Transduction,Endocrine & Metabolism,Lipid Metabolism,Neuroscience,Cell Type Marker,Neurodegenerative Diseases,Dopamine Signaling in Parkinson's Disease,Oligodendrocyte marker,GBA

    Molecular Weight

    29 kDa/50 kDa/54 kDa/57 kDa/59 kDa

    Gene ID

    2629

    UniProt

    P04062

    Pathways

    Cellular Glucan Metabolic Process
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