BSDC1 抗体 (C-Term)
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北京 101111
Quick Overview for BSDC1 抗体 (C-Term) (ABIN1537276)
抗原
See all BSDC1 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 397-425, 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 BSDC1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 397-425 amino acids from the C-terminal region of human BSDC1.
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亚型
- Ig Fraction
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anti-BSD Domain Containing 1 (BSDC1) (AA 84-133) antibody
BSDC1 适用: 人, 小鼠, Cow, 豚鼠, 马, 兔, Hamster, 猴, Pig WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-BSD Domain Containing 1 (BSDC1) (N-Term) antibodyBSDC1 适用: 人, 小鼠, 犬, 大鼠, 斑马鱼 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-BSD Domain Containing 1 (BSDC1) (N-Term) antibodyBSDC1 适用: 人, 小鼠, 犬, Cow, 豚鼠, 马, 兔, 大鼠 WB, IHC 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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储存方法
- BSDC1 Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
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有效期
- 6 months
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- BSDC1 (BSD Domain Containing 1 (BSDC1))
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别名
- BSDC1
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背景
- BSDC1 is a 430 amino acid protein encoded by a gene mapping to chromosome 1. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma.
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分子量
- 47163
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基因ID
- 55108
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NCBI登录号
- NP_001137360, NP_001137361, NP_001137362, NP_060515
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UniProt
- Q9NW68
抗原
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