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Arylsulfatase A Protein (ARSA) (Transcript Variant 1) (His tag)

Recombinant Arylsulfatase A protein expressed in HEK-293 Cells.
Catalog No. ABIN2714957
$420.00
Plus shipping costs $50.00, if applicable $20.00 dry ice
10 μg
Shipping to: United States
Delivery in 4 to 9 Business Days

Quick Overview for Arylsulfatase A Protein (ARSA) (Transcript Variant 1) (His tag) (ABIN2714957)

Target

See all Arylsulfatase A (ARSA) Proteins
Arylsulfatase A (ARSA)

Protein Type

Recombinant

Origin

  • 14
  • 3
Human

Source

  • 5
  • 4
  • 3
  • 2
  • 2
  • 1
HEK-293 Cells

Application

Antibody Production (AbP), Standard (STD)

Purity

> 95 % as determined by SDS-PAGE and Coomassie blue staining
  • Protein Characteristics

    Transcript Variant 1

    Purification tag / Conjugate

    This Arylsulfatase A protein is labelled with His tag.

    Characteristics

    • Recombinant human Arylsulfatase A (transcript variant 1) protein expressed in HEK293 cells.
    • Produced with end-sequenced ORF clone

    Endotoxin Level

    < 0.1 EU per μg protein as determined by LAL test
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  • Application Notes

    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays

    Comment

    The tag is located at the C-terminal.

    Restrictions

    For Research Use only
  • Concentration

    50 μg/mL

    Buffer

    20 mM Tris-HCl, 150 mM NaCl, pH 7.5. Avoid repeated freeze-thaw cycles. Stable for at least 3 months from receipt of products under proper storage and handling conditions.

    Storage

    -80 °C

    Storage Comment

    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target

    Arylsulfatase A (ARSA)

    Alternative Name

    Arylsulfatase A

    Background

    The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy (MLD), a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.

    Molecular Weight

    52.9 kDa

    NCBI Accession

    NP_000478
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