Arylsulfatase B antibody (C-Term)

Catalog No. ABIN7970356

The Rabbit Polyclonal anti-Arylsulfatase B antibody is suitable to detect Arylsulfatase B in samples from Mouse and Rat. It has been validated for WB.

Quick Overview for Arylsulfatase B antibody (C-Term) (ABIN7970356)

Target: Arylsulfatase B (ARSB)

Reactivity: Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase B antibody is un-conjugated

Application: Western Blotting (WB)

Grade: Carrier-free

Product Details anti-Arylsulfatase B Antibody

Binding Specificity: C-Term

Purpose: Anti-Arsb Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-Arsb Antibody. Tested in WB applications. This antibody reacts with Mouse, Rat.

Purification: Immunogen affinity purified.

Immunogen: A synthetic peptide corresponding to a sequence at the C-terminus of mouse Arsb, which shares 88.2% and 94.1% amino acid (aa) sequence identity with human and rat Arsb, respectively.

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Mouse, Rat

Restrictions: For Research Use only

Handling

Format: Lyophilized

Reconstitution: Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

Buffer: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.01 mg 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: Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for Arylsulfatase B

Target: Arylsulfatase B (ARSB)

Alternative Name: Arsb

Background:

Background: Arylsulfatase B encoded by this gene 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 targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene

Gene Full Name: arylsulfatase B

Molecular Weight: 66-70 kDa

Gene ID: 11881

UniProt: P50429

Pathways: Glycosaminoglycan Metabolic Process