ALG11 抗体 (AA 301-385)
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- 抗原 See all ALG11 抗体
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
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抗原表位
- AA 301-385
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适用
- 人
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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 ALG11 antibody is un-conjugated
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应用范围
- ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ALG11
- 亚型
- IgG
- Top Product
- Discover our top product ALG11 Primary Antibody
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- 应用备注
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ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- ALG11 (Asparagine-Linked Glycosylation 11, alpha-1,2-Mannosyltransferase Homolog (Yeast) (ALG11))
- 别名
- ALG11 (ALG11 产品)
- 别名
- UTP14C antibody, CDG1P antibody, GT8 antibody, RGD1564725 antibody, AI849156 antibody, AW492253 antibody, B230397C21 antibody, si:dkey-1h24.5 antibody, wu:fj04e04 antibody, asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase antibody, ALG11, alpha-1,2-mannosyltransferase antibody, ALG11, alpha-1,2-mannosyltransferase L homeolog antibody, asparagine-linked glycosylation 11 (alpha-1,2-mannosyltransferase) antibody, alg11 antibody, ALG11 antibody, alg11.L antibody, Alg11 antibody
- 背景
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Synonyms: Asparagine-linked glycosylation protein 11 homolog, AI849156, alg11, ALG11_HUMAN, Asparagine-linked glycosylation 11, Asparagine-linked glycosylation 11, alpha-1,2-mannosyltransferase homolog yeast, GT8, UTP14C.
Background: Mannosyltransferase involved in the last steps of the synthesis of Man5GlcNAc(2)-PP-dolichol core oligosaccharide on the cytoplasmic face of the endoplasmic reticulum. Catalyzes the addition of the 4th and 5th mannose residues to the dolichol-linked oligosaccharide chain.Involvement in disease:Defects in ALG11 are the cause of congenital disorder of glycosylation type 1P (CDG1P). A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions.
- 基因ID
- 440138
- 途径
- SARS-CoV-2 Protein Interactome
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