WBSCR22 Antibody Summary
| Immunogen |
WBSCR22 (NP_059998.2, 1 a.a. ~ 281 a.a) full-length human protein.MASRGRRPEHGGPPELFYDETEARKYVRNSRMIDIQTRMAGRALELLYLPENKPCYLLDIGCGTGLSGSYLSDEGHYWVGLDISPAMLDEAVDREIEGDLLLGDMGQGIPFKPGTFDGCISISAVQWLCNANKKSENPAKRLYCFFASLFSVLVRGSRAVLQLYPENSEQLELITTQATKAGFSGGMVVDYPNSAKAKKFYLCLFSGPSTFIPEGLSENQDEVEPRESVFTNERFPLRMSRRGMVRKSRAWVLEK
|
| Specificity |
WBSCR22 – Williams Beuren syndrome chromosome region 22,
|
| Clonality |
Polyclonal
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| Host |
Mouse
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| Gene |
WBSCR22
|
| Purity |
Protein A purified
|
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Applications/Dilutions
| Dilutions |
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| Application Notes |
Antibody reactive against recombinant protein with GST tag on ELISA and western blot and also on transfected lysate in western blot. GST tag alone is used as a negative control. It is also useful for immunofluoresence.
|
Reactivity Notes
Human.
Packaging, Storage & Formulations
| Storage |
Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
|
| Buffer |
PBS (pH 7.4)
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| Preservative |
No Preservative
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| Purity |
Protein A purified
|
Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for WBSCR22 Antibody
- EC 2.1.1.-
- FLJ44236
- HASJ4442
- HUSSY-3
- MGC19709
- MGC2022
- MGC5140
- PP3381
- WBMT
- Williams Beuren syndrome chromosome region 22 protein
- Williams Beuren syndrome chromosome region 22
- Williams-Beuren candidate region putative methyltransferase
- Williams-Beuren syndrome chromosomal region 22 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. [provided by RefSeq]