-
- 抗原 See all WBSCR22 抗体
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
-
抗原表位
- AA 253-281, C-Term
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This WBSCR22 antibody is un-conjugated
-
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
-
-
- 应用备注
- WB: 1:1000
- 限制
- 仅限研究用
-
- 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
-
-
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).
: "
-
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).
-
- 抗原
- WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
- 别名
- WBSCR22 (WBSCR22 产品)
- 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
-