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GALE antibody (N-Term)

The Rabbit Polyclonal anti-GALE antibody is suitable to detect GALE in samples from Human, Rat, Mouse, Dog, Cow, Pig, Rabbit and Guinea Pig. It has been validated for WB.
Catalog No. ABIN2785690
$483.54
Plus shipping costs $50.00
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for GALE antibody (N-Term) (ABIN2785690)

Target

See all GALE Antibodies
GALE (UDP-Galactose-4-Epimerase (GALE))

Reactivity

  • 64
  • 18
  • 16
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Rat, Mouse, Dog, Cow, Pig, Rabbit, Guinea Pig

Host

  • 58
  • 6
Rabbit

Clonality

  • 60
  • 4
Polyclonal

Conjugate

  • 25
  • 5
  • 4
  • 4
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This GALE antibody is un-conjugated

Application

  • 53
  • 24
  • 17
  • 13
  • 13
  • 6
  • 5
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 12
    • 9
    • 8
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    N-Term

    Purpose

    GALE Antibody - N-terminal region

    Sequence

    AEKVLVTGGA GYIGSHTVLE LLEAGYLPVV IDNFHNAFRG GGSLPESLRR

    Predicted Reactivity

    Cow: 93%, Dog: 86%, Guinea Pig: 86%, Human: 100%, Mouse: 91%, Pig: 91%, Rabbit: 92%, Rat: 91%

    Characteristics

    This is a rabbit polyclonal antibody against GALE. It was validated on Western Blot using a cell lysate as a positive control.

    Purification

    Affinity Purified

    Immunogen

    The immunogen is a synthetic peptide directed towards the N terminal region of human GALE
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Comment

    We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP54393-100UG

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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.

    Handling Advice

    prevent freeze-thaw cycles

    Storage

    4 °C,-20 °C

    Storage Comment

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

    GALE (UDP-Galactose-4-Epimerase (GALE))

    Alternative Name

    GALE

    Background

    Background Information: GALE is an UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). This gene encodes UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild ('peripheral' form) to severe ('generalized' form). Multiple alternatively spliced transcripts encoding the same protein have been identified.

    Gene Name: UDP-galactose-4-epimerase

    Alternative Symbols: SDR1E1

    Protein Name: UDP-glucose 4-epimerase

    Molecular Weight

    38kDa

    Gene ID

    2582

    NCBI Accession

    NP_001008217

    UniProt

    Q14376

    Pathways

    Response to Water Deprivation, Cellular Glucan Metabolic Process
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