Arylsulfatase B antibody (C-Term)

Catalog No. ABIN359624

Product Details anti-Arylsulfatase B Antibody

Target: Arylsulfatase B (ARSB)

Binding Specificity: C-Term

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase B antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Specificity: This antibody reacts to ARSB.

Purification: Prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS

Immunogen: This antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the C-terminal region of human ARSB.

Isotype: Ig Fraction

Application Details

Application Notes: ELISA: 1/1,000. Western blot: 1/50 - 1/100.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: 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.

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at-20 °C for longer.

Target Details for Arylsulfatase B

Target: Arylsulfatase B (ARSB)

Alternative Name: Arylsulfatase B (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: 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.Synonyms: ARSB, ASB, G4S, N-acetylgalactosamine-4-sulfatase

Gene ID: 411, 9606

UniProt: P15848

Pathways: Glycosaminoglycan Metabolic Process