SVOPL 抗体 (Middle Region)
The 兔 多克隆 anti-SVOPL antibody (ABIN955017) specifically detects SVOPL in WB 和 EIA.
The antibody is reactive with 人 samples.
1 image
产品编号 ABIN955017
发货至:
中国
Contact our Customer Service for availability and price in your country.
Contact Info
Our Local Distributor
中国
北京 101111
北京 101111
No. 88 KeChuang 6th Street
Beijing Economic Technological Development Area
Room 801-803
Quick Overview for SVOPL 抗体 (Middle Region) (ABIN955017)
抗原
SVOPL
(SVOP-Like (SVOPL))
适用
人
宿主
兔
克隆类型
多克隆
标记
This SVOPL antibody is un-conjugated
应用范围
Western Blotting (WB), Enzyme Immunoassay (EIA)
-
-
抗原表位
- AA 240-269, Middle Region
-
特异性
- This antibody detects SVOPL (Center).
-
交叉反应 （详细）
- Species reactivity (tested):Human
-
纯化方法
- Protein A column followed by peptide affinity purification
-
免疫原
- KLH conjugated synthetic peptide between 240-269 amino acids from the Central region of human SVOPL
-
亚型
- Ig Fraction
-
-
anti-SVOP-Like (SVOPL) (AA 73-129) antibody
SVOPL 适用: 人 ELISA, WB, IF 宿主: 兔 Polyclonal unconjugated
-
-
应用备注
- Optimal working dilution should be determined by the investigator.
-
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 0.25 mg/mL
-
缓冲液
- PBS, 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.
-
注意事项
- Avoid repeated freezing and thawing.
-
储存条件
- 4 °C/-20 °C
-
储存方法
- Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.
-
-
- SVOPL (SVOP-Like (SVOPL))
-
别名
- SVOPL
-
背景
- SVOPL (putative transporter SVOPL), also known as SV2-related protein-like, is a 492 amino acid multi-pass membrane protein belonging to the major facilitator superfamily. SVOPL is a paralog to synaptic vesicle protein (SVOP) that exists as two alternatively spliced isoforms. The gene encoding SVOPL maps to human chromosome 7q34. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up approximately 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Deletions of portions of the q arm of chromosome 7 are linked to myeloid disorders, including acute myelogenous leukemia and myelodysplasia.Synonyms: Putative transporter
-
分子量
- Molecular Weight: 53991 Da
-
基因ID
- 136306
-
NCBI登录号
- NP_001132928
抗原
-
You are here:
