產(chǎn)品名稱 Williams-Beuren Syndrome Chromosomal Region 22 Protein (WBSCR22) Antibody
產(chǎn)品貨號(hào) Catalogue No: abx031474
產(chǎn)品價(jià)格 現(xiàn)貨詢價(jià),電話:010-67529703
產(chǎn)品規(guī)格 Available Options * Size: 80 μl 400 μl
產(chǎn)品品牌 abbexa
產(chǎn)品概述
產(chǎn)品詳情
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.
Target WBSCR22
Reactivity Human
Host Rabbit
Clonality Polyclonal
Tested Applications WB
Recommended dilutions Optimal dilutions/concentrations should be determined by the end user.
Immunogen KLH-conjugated synthetic peptide between 253-281 amino acids from the C-terminal region of human WBSCR22.
Purification Purified through a protein A column, followed by peptide affinity purification.
Isotype IgG
Conjugation Unconjugated
Storage Aliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
Swiss Prot O43709
Gene Symbol WBSCR22
Buffer PBS containing 0.09% sodium azide.
UNSPSC Code 12352203
Availability Shipped within 5-10 working days.
Note This product is for research use only.
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