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Arylsulfatase B antibody (C-Term)

The Rabbit Polyclonal anti-Arylsulfatase B antibody has been validated for WB and IHC (p). It is suitable to detect Arylsulfatase B in samples from Human.
Catalog No. ABIN391670

Quick Overview for Arylsulfatase B antibody (C-Term) (ABIN391670)

Target

See all Arylsulfatase B (ARSB) Antibodies
Arylsulfatase B (ARSB)

Reactivity

  • 37
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 33
  • 4
  • 1
Rabbit

Clonality

  • 35
  • 3
Polyclonal

Conjugate

  • 21
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Arylsulfatase B antibody is un-conjugated

Application

  • 28
  • 19
  • 7
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  • 4
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB18353
  • Binding Specificity

    • 8
    • 7
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 464-493, C-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogen

    This ARSB antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 464-493 amino acids from the C-terminal region of human ARSB.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. IHC-P: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    Arylsulfatase B (ARSB)

    Alternative Name

    ARSB

    Background

    ARSB belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targetted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B.

    Molecular Weight

    59687

    Gene ID

    411

    NCBI Accession

    NP_000037, NP_942002

    UniProt

    P15848

    Pathways

    Glycosaminoglycan Metabolic Process
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