WBSCR27 antibody (N-Term)

Catalog No. ABIN955542

This anti-WBSCR27 antibody is a Rabbit Polyclonal antibody detecting WBSCR27 in WB, IHC (p) and EIA. Suitable for Human.

Quick Overview for WBSCR27 antibody (N-Term) (ABIN955542)

Target: WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This WBSCR27 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Product Details anti-WBSCR27 Antibody

Binding Specificity: AA 12-42, N-Term

Specificity: This antibody detects WBSCR27 (N-term).

Cross-Reactivity (Details): Species reactivity (tested):Human

Purification: Protein A column followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 12-42 amino acids from the N-terminal region of human WBSCR27

Isotype: Ig Fraction

Application Details

Application Notes: Optimal working dilution should be determined by the investigator.

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 at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Target Details for WBSCR27

Target: WBSCR27 (Williams Beuren Syndrome Chromosome Region 27 (WBSCR27))

Alternative Name: WBSCR27

Background: WBSCR27 encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23Synonyms: Williams-Beuren syndrome chromosomal region 27 protein

Gene ID: 155368

NCBI Accession: NP_689772