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GLT8D1 antibody (FITC)

The Rabbit Polyclonal anti-GLT8D1 antibody has been validated for WB and IF (p). It is suitable to detect GLT8D1 in samples from Human, Mouse and Rat.
Catalog No. ABIN1403402

Quick Overview for GLT8D1 antibody (FITC) (ABIN1403402)

Target

See all GLT8D1 Antibodies
GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

Reactivity

  • 36
  • 19
  • 18
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Mouse, Rat

Host

  • 36
Rabbit

Clonality

  • 36
Polyclonal

Conjugate

  • 13
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GLT8D1 antibody is conjugated to FITC

Application

  • 31
  • 14
  • 12
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human GLT8D1

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

    Expiry Date

    12 months
  • Target

    GLT8D1 (Glycosyltransferase 8 Domain Containing 1 (GLT8D1))

    Alternative Name

    GLT8D1

    Background

    Synonyms: MGC94018, Da2 24, GALA4A, Glycosyltransferase 8 domain containing 1, Glycosyltransferase 8 domain-containing protein 1, Glycosyltransferase AD 017, MSTP139, GL8D1_HUMAN.

    Background: GLT8D1 is a 371 amino acid single-pass type II transmembrane protein that is expressed by a gene residing on human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3. There are two isoforms of GLT8D1 that are produced as a result of alternative splicing events.

    Gene ID

    55830
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