WBSCR22 抗体 (AA 1-233)
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北京 101111
Quick Overview for WBSCR22 抗体 (AA 1-233) (ABIN1885820)
抗原
See all WBSCR22 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-233
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein fragment contain a sequence corresponding to a region within amino acids 1 and 233 of Human WBSCR22
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anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (Center) antibody
WBSCR22 适用: 人, 小鼠 WB, IF, IP, IHC (p), ICC 宿主: 兔 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (AA 1-110) antibodyWBSCR22 适用: 人 WB, IF, ELISA, IP 宿主: 小鼠 Monoclonal 2E12 unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (AA 1-281) antibodyWBSCR22 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (AA 1-281) antibodyWBSCR22 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) antibodyWBSCR22 适用: 人, 大鼠 WB, IF, IHC, IC 宿主: 兔 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (AA 200-249) antibodyWBSCR22 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (C-Term) antibodyWBSCR22 适用: 人, 大鼠, 小鼠, 犬, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (AA 253-281), (C-Term) antibodyWBSCR22 适用: 人 WB 宿主: 兔 Polyclonal RB42713 unconjugated
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应用备注
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Suggested dilutions:
Western blotting: 1.500-1.3000
Immunohistochemistry: 1.100-1.250 -
限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- 0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
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储存液
- Thimerosal (Merthiolate)
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注意事项
- Biohazard Informations: This product contains thimerosal which is hazardous.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
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- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
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别名
- WBSCR22
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背景
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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]
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分子量
- 32 kDa
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基因ID
- 114049
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NCBI登录号
- NP_059998, NM_017528
抗原
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