WBSCR22 抗体 (C-Term)
(4 references)-
- 抗原 See all WBSCR22 抗体
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
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抗原表位
- AA 253-281, C-Term
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This WBSCR22 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 预测反应
- B, M
- 纯化方法
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- 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.
- 克隆位点
- RB42713
- 亚型
- Ig Fraction
- Top Product
- Discover our top product WBSCR22 Primary Antibody
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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) antibodyWBSCR22 适用: 人, 大鼠 IF, IHC 宿主: 兔 Polyclonal 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) (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
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- 应用备注
- WB: 1:1000
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 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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- 抗原
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- 别名
- WBSCR22 (WBSCR22 产品)
- 别名
- 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
- 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.
- 分子量
- 31880
- NCBI登录号
- NP_001189489, NP_059998
- UniProt
- O43709
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