WBSCR22 抗体 (AA 1-281)
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北京 101111
Quick Overview for WBSCR22 抗体 (AA 1-281) (ABIN6150175)
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 1-281
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序列
- MASRGRRPEH GGPPELFYDE TEARKYVRNS RMIDIQTRMA GRALELLYLP ENKPCYLLDI GCGTGLSGSY LSDEGHYWVG LDISPAMLDE AVDREIEGDL LLGDMGQGIP FKPGTFDGCI SISAVQWLCN ANKKSENPAK RLYCFFASLF SVLVRGSRAV LQLYPENSEQ LELITTQATK AGFSGGMVVD YPNSAKAKKF YLCLFSGPST FIPEGLSENQ DEVEPRESVF TNERFPLRMS RRGMVRKSRA WVLEKKERHR RQGREVRPDT QYTGRKRKPR F
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交叉反应
- 人, 大鼠
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产品特性
- Polyclonal Antibodies
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-281 of human WBSCR22 (NP_059998.2).
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亚型
- IgG
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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) antibodyWBSCR22 适用: 人, 大鼠 WB, IF, IHC, IC 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 200-249) antibodyWBSCR22 适用: 人 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
- WB,1:500 - 1:2000,IF,1:50 - 1:100
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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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
- 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.,BUD23,HASJ4442,HUSSY-3,MERM1,PP3381,WBMT,WBSCR22,Epigenetics & Nuclear Signaling,Cancer,Signal Transduction,Endocrine & Metabolism,Amino acid metabolism,WBSCR22
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分子量
- 24 kDa/31 kDa/33 kDa
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基因ID
- 114049
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UniProt
- O43709
抗原
-
