ABHD11 antibody (AA 130-210)

Catalog No. ABIN7213426

The Rabbit Polyclonal anti-ABHD11 antibody is suitable to detect ABHD11 in samples from Human and Mouse. It has been validated for ELISA and WB.

Quick Overview for ABHD11 antibody (AA 130-210) (ABIN7213426)

Target: ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ABHD11 antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-ABHD11 Antibody

Binding Specificity: AA 130-210

Purpose: Rabbit Anti-ABHD11 Polyclonal Antibody

Specificity: ABHD11 Polyclonal Antibody detects endogenous levels of ABHD11 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 ABHD11 at AA range: 130-210

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 1:20000,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 ABHD11

Target: ABHD11 (Abhydrolase Domain Containing 11 (ABHD11))

Alternative Name: ABHD11

Background: ABHD11, WB SCR21, PP1226, Abhydrolase domain-containing protein 11, Williams-Beuren syndrome chromosomal region 21 proteinABHD11 encodes a protein (abhydrolase domain containing 11) containing an alpha/beta hydrolase fold domain. ABHD11 is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.

Molecular Weight: 32kD

Gene ID: 83451

UniProt: Q8NFV4