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WBSCR22 antibody
WBSCR22
Reactivity: Human, Rat
IF, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-WBSCR22 Antibody
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Target
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WBSCR22
(Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
Reactivity
All reactivities for WBSCR22 antibodies
Human, Rat
Host
All hosts for WBSCR22 antibodies
Rabbit
Clonality
All clonalities for WBSCR22 antibodies
Polyclonal
Conjugate
All conjugates for WBSCR22 antibodies
This WBSCR22 antibody is un-conjugated
Application
All applications for WBSCR22 antibodies
Immunofluorescence (IF), Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant fusion protein of human WBSCR22 (NP_059998.2).
Isotype
IgG
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Discover our top product WBSCR22 Primary Antibody
Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200 IF 1:50-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
1 mg/mL
Buffer
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for WBSCR22
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Target
WBSCR22
(Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
Alternative Name
WBSCR22 (WBSCR22 Products )
Synonyms
MGC82375 antibody, wbmt antibody, pp3381 antibody, hussy-3 antibody, hasj4442 antibody, zgc:162306 antibody, HASJ4442 antibody, HUSSY-3 antibody, MERM1 antibody, PP3381 antibody, WBMT antibody, 1110003N24Rik antibody, Williams-Beuren syndrome chromosome region 22 antibody, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog antibody, BUD23, rRNA methyltransferase and ribosome maturation factor antibody, williams Beuren syndrome chromosome region 22 antibody, hypothetical protein antibody, WBSCR22 antibody, bud23.L antibody, bud23 antibody, CpipJ_CPIJ001394 antibody, PAAG_00857 antibody, MCYG_07273 antibody, PGTG_07527 antibody, PGTG_12505 antibody, BUD23 antibody, Bud23 antibody
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.
Gene ID
114049
UniProt
O43709
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