WBSCR22 Protein (His tag)

Catalog No. ABIN2735489

Product Details

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Protein Type: Recombinant

Origin: Human

Source: Escherichia coli (E. coli)

Purification tag / Conjugate: This WBSCR22 protein is labelled with His tag.

Application: Antibody Production (AbP), Standard (STD)

Characteristics:

• Recombinant human WBSCR22 (full length, N-term HIS tag, transcript variant 2) protein expressed in E.coli.
• Produced with end-sequenced ORF clone

Purity: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Application Details

Application Notes: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Comment:

The tag is located at the N-terminal.

Restrictions: For Research Use only

Handling

Concentration: 50 μg/mL

Buffer: 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.

Storage: -80 °C

Storage Comment: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Target Details

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Alternative Name: Wbscr22 (WBSCR22 Products)

Synonyms: MGC82375 Protein, wbmt Protein, pp3381 Protein, hussy-3 Protein, hasj4442 Protein, zgc:162306 Protein, HASJ4442 Protein, HUSSY-3 Protein, MERM1 Protein, PP3381 Protein, WBMT Protein, 1110003N24Rik Protein, Williams-Beuren syndrome chromosome region 22 Protein, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog Protein, BUD23, rRNA methyltransferase and ribosome maturation factor Protein, williams Beuren syndrome chromosome region 22 Protein, hypothetical protein Protein, WBSCR22 Protein, bud23.L Protein, bud23 Protein, CpipJ_CPIJ001394 Protein, PAAG_00857 Protein, MCYG_07273 Protein, PGTG_07527 Protein, PGTG_12505 Protein, BUD23 Protein, Bud23 Protein

Background: This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.

Molecular Weight: 31.7 kDa

NCBI Accession: NP_059998