SATL1 抗体 (C-Term)
This anti-SATL1 antibody is a 兔 多克隆 antibody detecting SATL1 in WB 和 EIA. Suitable for 人.
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产品编号 ABIN954676
发货至:
中国
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Quick Overview for SATL1 抗体 (C-Term) (ABIN954676)
抗原
SATL1
(Spermidine/spermine N1-Acetyl Transferase-Like 1 (SATL1))
适用
人
宿主
兔
克隆类型
多克隆
标记
This SATL1 antibody is un-conjugated
应用范围
Western Blotting (WB), Enzyme Immunoassay (EIA)
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抗原表位
- AA 322-352, C-Term
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特异性
- Recognizes SATL1 (C-term)
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纯化方法
- Protein A column followed by peptide Affinity purification
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免疫原
- KLH conjugated synthetic peptide between 322-352 amino acids from the C-terminal region of Human SATL1 (NP_001012998.2) Genename: SATL1
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亚型
- Ig Fraction
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anti-Spermidine/spermine N1-Acetyl Transferase-Like 1 (SATL1) (AA 322-351), (C-Term) antibody
SATL1 适用: 人 WB 宿主: 兔 Polyclonal RB28405 unconjugated
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应用备注
- Optimal working dilution should be determined by the investigator.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.25 mg/mL
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缓冲液
- PBS with 0.09 % (W/V) Sodium Azide as preservative
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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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注意事项
- Avoid repeated freezing and thawing.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- SATL1 (Spermidine/spermine N1-Acetyl Transferase-Like 1 (SATL1))
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别名
- SATL1
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背景
- SATL1 (spermine N(1)-acetyltransferase-like protein 1) is a 508 amino acid protein that contains one N-acetyltransferase domain, and belongs to the acetyltransferase family. Existing as two alternatively spliced isoforms, the SATL1 gene is conserved in chimpanzee, dog, cow, mouse and rat, and maps to human chromosome Xq21.1. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.Synonyms: Spermidine/spermine N(1)-acetyltransferase-like protein 1
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基因ID
- 340562
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NCBI登录号
- NP_001012998
抗原
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