DPAGT1 抗体 (AA 286-315)
(1 reference)Quick Overview for DPAGT1 抗体 (AA 286-315) (ABIN653925)
抗原
See all DPAGT1 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 286-315
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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 DPAGT1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 286-315 amino acids from the Central region of human DPAGT1.
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亚型
- Ig Fraction
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anti-Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1) (C-Term) antibody
DPAGT1 适用: 人, 小鼠, 大鼠, 犬, 豚鼠, 马, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1) (AA 301-408) antibodyDPAGT1 适用: 小鼠, 大鼠 WB, ELISA, IF (cc), IF (p), IHC (p), ICC, IHC (fro) 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1) (N-Term) antibodyDPAGT1 适用: 人, 小鼠 WB, IHC (p), EIA, IF 宿主: 兔 Polyclonal unconjugated
anti-Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1) (AA 296-377) antibodyDPAGT1 适用: 人 ELISA 宿主: 小鼠 Monoclonal 1G1 unconjugated
anti-Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1) (AA 28-57), (N-Term) antibodyDPAGT1 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB32141 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
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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有效期
- 6 months
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: "Congenital myasthenic syndrome caused by mutations in DPAGT." in: Neuromuscular disorders : NMD, Vol. 25, Issue 3, pp. 253-6, (2015) (PubMed).
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: "Congenital myasthenic syndrome caused by mutations in DPAGT." in: Neuromuscular disorders : NMD, Vol. 25, Issue 3, pp. 253-6, (2015) (PubMed).
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- DPAGT1 (Dolichyl-Phosphate (UDP-N-Acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P Transferase) (DPAGT1))
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别名
- DPAGT1
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背景
- DPAGT1 encoded by this gene is an enzyme that catalyzes the first step in the dolichol-linked oligosaccharide pathway for glycoprotein biosynthesis. This enzyme belongs to the glycosyltransferase family 4. This protein is an integral membrane protein of the endoplasmic reticulum. The congenital disorder of glycosylation type Ij is caused by mutation in the gene encoding this enzyme.
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分子量
- 46090
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基因ID
- 1798
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NCBI登录号
- NP_001373
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UniProt
- Q9H3H5
抗原
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