Arylsulfatase E antibody (AA 120-200)

Catalog No. ABIN7222378

The Rabbit Polyclonal anti-Arylsulfatase E antibody (ABIN7222378) specifically detects Arylsulfatase E in ELISA and WB. The antibody is reactive with Human samples.

Quick Overview for Arylsulfatase E antibody (AA 120-200) (ABIN7222378)

Target: Arylsulfatase E (ARSE)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Arylsulfatase E antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-Arylsulfatase E Antibody

Binding Specificity: AA 120-200

Purpose: Rabbit Anti-Arylsulfatase E Polyclonal Antibody

Specificity: Arylsulfatase E Polyclonal Antibody detects endogenous levels of Arylsulfatase E protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: Synthesized peptide derived from the Internal region of human Arylsulfatase E at AA range: 120-200

Isotype: IgG

Application Details

Application Notes: Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000,ELISA 1:10000,Not yet tested in other applications.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 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: -20 °C

Storage Comment: Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.

Expiry Date: 12 months

Target Details for Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Alternative Name: Arylsulfatase E

Background: ARSE, Arylsulfatase E, ASEArylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome.

Molecular Weight: 65kD

Gene ID: 415

UniProt: P51690