GLTPD2 抗体 (Alexa Fluor 594)
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- 抗原 See all GLTPD2 products
- GLTPD2 (Glycolipid Transfer Protein Domain Containing 2 (GLTPD2))
- 适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This GLTPD2 antibody is conjugated to Alexa Fluor 594
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human GLTPD2
- 亚型
- IgG
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anti-Glycolipid Transfer Protein Domain Containing 2 (GLTPD2) (AA 151-200) antibody
GLTPD2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycolipid Transfer Protein Domain Containing 2 (GLTPD2) (AA 36-85) antibodyGLTPD2 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 1:50-200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 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
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- GLTPD2 (Glycolipid Transfer Protein Domain Containing 2 (GLTPD2))
- 别名
- GLTPD2 (GLTPD2 产品)
- 别名
- C730027E14Rik antibody, RP23-122P1.9 antibody, RGD1560459 antibody, glycolipid transfer protein domain containing 2 antibody, GLTPD2 antibody, Gltpd2 antibody
- 背景
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Synonyms: glycolipid transfer protein domain-containing protein 2, Glycolipid transfer protein domain containing 2, GLTD2_HUMAN.
Background: The GLTP (glycolipid transfer protein) superfamily is defined by a unique lipid transfer/binding fold (GLTP fold) that accelerate glycolipid intermembrane transfer. GLTPD2 is a 291 amino acid protein that belongs to the GLTP family. The gene encoding GLTPD2 maps to human chromosome 17, which comprises over 2.5 % of the human genome and encodes over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, p53 and BRCA1. Malfunction or loss of p53 expression is associated with malignant cell growth and Li-Fraumeni syndrome. Neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth are both linked to mutations on chromosome 17. Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are also associated with chromosome 17.
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