T-Box 1 抗体
Quick Overview for T-Box 1 抗体 (ABIN7254388)
抗原
See all T-Box 1 (TBX1) 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Antigen affinity purification
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免疫原
- Synthetic peptide of human TBX1
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亚型
- IgG
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anti-T-Box 1 (TBX1) (AA 327-356), (C-Term) antibody
TBX1 适用: 人 WB, IF, IHC (p) 宿主: 兔 Polyclonal RB22154 unconjugated
anti-T-Box 1 (TBX1) (C-Term) antibodyTBX1 适用: 人 WB, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (C-Term) antibodyTBX1 适用: 人 WB, ELISA, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (AA 396-445) antibodyTBX1 适用: 人, 小鼠, 大鼠, 豚鼠, 兔, 犬 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (C-Term) antibodyTBX1 适用: 人 WB, IHC, IF, IC 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (C-Term) antibodyTBX1 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (AA 22-107) antibodyTBX1 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (AA 327-356) antibodyTBX1 适用: 人 WB, IHC, IF, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (AA 324-373) antibodyTBX1 适用: 人, 小鼠, 大鼠, 豚鼠, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-T-Box 1 (TBX1) (C-Term) antibodyTBX1 适用: 人, 小鼠, 大鼠, 豚鼠, 兔, 犬 WB, IHC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:500-1:2000, IHC 1:25-1:100, ELISA 1:5000-1:10000
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.7 mg/mL
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缓冲液
- PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4
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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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- T-Box 1 (TBX1)
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别名
- TBX1
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背景
- This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.
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分子量
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Observed_MW: Refer to figures
Calculated_MW: 43 kDa
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UniProt
- O43435
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途径
- Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation
抗原
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