WBSCR22 抗体 (C-Term)
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北京 101111
Quick Overview for WBSCR22 抗体 (C-Term) (ABIN1881998)
抗原
See all WBSCR22 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 253-281, C-Term
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预测反应
- B, M
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纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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免疫原
- This WBSCR22 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 253-281 amino acids from the C-terminal region of human WBSCR22.
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亚型
- Ig Fraction
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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
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应用备注
- WB: 1:1000
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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
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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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
- 4 °C,-20 °C
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有效期
- 6 months
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: "hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes." in: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).
: "Nucleolar proteome dynamics." in: Nature, Vol. 433, Issue 7021, pp. 77-83, (2005) (PubMed).
: "Identification of additional transcripts in the Williams-Beuren syndrome critical region." in: Human genetics, Vol. 110, Issue 5, pp. 429-38, (2002) (PubMed).
: "Characterization of 16 novel human genes showing high similarity to yeast sequences." in: Yeast (Chichester, England), Vol. 18, Issue 1, pp. 69-80, (2001) (PubMed).
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: "hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes." in: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).
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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.
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分子量
- 31880
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NCBI登录号
- NP_001189489, NP_059998
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UniProt
- O43709
抗原
-
