Arylsulfatase B antibody (C-Term)

Catalog No. ABIN2457880

Product Details anti-Arylsulfatase B Antibody

Target: Arylsulfatase B (ARSB)

Binding Specificity: C-Term

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase B antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC), Immunofluorescence (IF)

Specificity: ARSB antibody is human, mouse and rat reactive. At least two isoforms of ARSB are known to exist, this antibody only recognizes the longest isoform.

Purification: ARSB Antibody is affinity chromatography purified via peptide column.

Immunogen: ARSB antibody was raised against a 16 amino acid peptide near the carboxy terminus of human ARSB

Isotype: IgG

Application Details

Application Notes: ARSB antibody can be used for detection of ARSB by Western blot at 1 - 2 μg/mL.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS containing 0.02 % 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: Can be stored at 4 °C for three months and -20 °C, stable for up to one year.

Target Details for Arylsulfatase B

Target: Arylsulfatase B (ARSB)

Alternative Name: ARSB (ARSB Products)

Synonyms: ASB antibody, G4S antibody, MPS6 antibody, 1110007C02Rik antibody, AI480648 antibody, As-1 antibody, As-1r antibody, As-1s antibody, As-1t antibody, As1 antibody, As1-r antibody, As1-s antibody, As1-t antibody, Asr-1 antibody, Ast-1 antibody, ARSB antibody, arylsulfatase B antibody, arylsulfatase antibody, arylsulfatase b antibody, ARSB antibody, Arsb antibody, RB348 antibody, LOC5566067 antibody, CpipJ_CPIJ011047 antibody, VDBG_03275 antibody, arsb antibody, LOC5579667 antibody

Background: Aryl sulfatase B (ARSB) forms a homodimer that hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate (1). ARSB localizes to the lysozyme as well as to the extracellular matrix (2). Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B (3), and can be treated with exogenous ARSB (4).

Molecular Weight: Predicted: 59 kDa

Observed: 57kDa

Gene ID: 411

NCBI Accession: NP_000037

UniProt: P15848

Pathways: Glycosaminoglycan Metabolic Process