ALG1 抗体 (C-Term)
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- 抗原 See all ALG1 抗体
- ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))
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抗原表位
- C-Term
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适用
- 人, 小鼠, 大鼠, 兔, Cow, 犬, 豚鼠
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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 ALG1 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- VKHEENGLVF EDSEELAAQL QMLFSNFPDP AGKLNQFRKN LRESQQLRWD
- 预测反应
- Cow: 86%, Dog: 93%, Guinea Pig: 92%, Human: 100%, Mouse: 86%, Rabbit: 86%, Rat: 92%
- 产品特性
- This is a rabbit polyclonal antibody against ALG1. It was validated on Western Blot.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the C-terminal region of human ALG1
- Top Product
- Discover our top product ALG1 Primary Antibody
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- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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 repeat freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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A severe human metabolic disease caused by deficiency of the endoplasmatic mannosyltransferase hALG11 leads to congenital disorder of glycosylation-Ip." in: Human molecular genetics, Vol. 19, Issue 8, pp. 1413-24, (2010) (PubMed).
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- 抗原
- ALG1 (Chitobiosyldiphosphodolichol beta-Mannosyltransferase (ALG1))
- 别名
- ALG1 (ALG1 产品)
- 别名
- CDG1K antibody, HMAT1 antibody, HMT-1 antibody, HMT1 antibody, MT-1 antibody, Mat-1 antibody, hMat-1 antibody, zgc:66221 antibody, wu:fi34b12 antibody, alg1 antibody, hmat1 antibody, hmt1 antibody, ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase antibody, asparagine-linked glycosylation 1 (beta-1,4-mannosyltransferase) antibody, Beta-mannosyltransferase antibody, ALG1, chitobiosyldiphosphodolichol beta-mannosyltransferase L homeolog antibody, ALG1 antibody, Alg1 antibody, alg1 antibody, alg1.L antibody
- 背景
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The enzyme encoded by this gene catalyzes the first mannosylation step in the biosynthesis of lipid-linked oligosaccharides. This gene is mutated in congenital disorder of glycosylation type Ik.
Alias Symbols: HMT1, MT-1, CDG1K, HMAT1, HMT-1, Mat-1, hMat-1
Protein Size: 353 - 分子量
- 38 kDa
- 基因ID
- 56052
- NCBI登录号
- NM_019109, NP_061982
- UniProt
- B4DP08
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