Homeobox D13 抗体
-
- 抗原 See all Homeobox D13 (HOXD13) 抗体
- Homeobox D13 (HOXD13)
-
适用
- 人
-
宿主
- 兔
-
克隆类型
- 多克隆
-
标记
- This Homeobox D13 antibody is un-conjugated
-
应用范围
- Western Blotting (WB)
- 交叉反应
- 人
- 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Recombinant protein encompassing a sequence within the center region of human HOXD13. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product HOXD13 Primary Antibody
-
-
- 应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- 说明
-
Positive Control: Jurkat , Raji , NCI-H929
- 限制
- 仅限研究用
-
- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 1XPBS ( pH 7), 20 % Glycerol, 0.025 % ProClin 300
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
-
- 抗原
- Homeobox D13 (HOXD13)
- 别名
- homeobox D13 (HOXD13 产品)
- 别名
- XHoxd13 antibody, BDE antibody, BDSD antibody, HOX4I antibody, SPD antibody, Hox-4.8 antibody, spdh antibody, hoxd-13 antibody, hoxd13 antibody, zgc:110511 antibody, homeobox D13 antibody, homeobox D13 S homeolog antibody, homeobox D13a antibody, homeo box D13 antibody, HOXD13 antibody, hoxd13.S antibody, Hoxd13 antibody, hoxd13a antibody
- 背景
- Homeobox D13 , BDE , BDSD , HOX4I , SPD , SPD1,This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly. [provided by RefSeq]
- 分子量
- 36 kDa
- 基因ID
- 3239
- UniProt
- P35453
- 途径
- Synaptic Membrane
-