Arylsulfatase E antibody (AA 120-200)

Catalog No. ABIN7222378

This anti-Arylsulfatase E antibody is a Rabbit Polyclonal antibody detecting Arylsulfatase E in ELISA and WB. Suitable for Human.

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: 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.

Comment:

Primary Antibody

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 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.

Target Details for Arylsulfatase E

Target: Arylsulfatase E (ARSE)

Alternative Name: Arylsulfatase E

Background: Rabbit Anti-Arylsulfatase E Polyclonal Antibody,ARSE, Arylsulfatase E, ASE,Arylsulfatase 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.,Arylsulfatase E

Gene ID: 415

UniProt: P51690