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- 抗原 See all HGSNAT 抗体
- HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))
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抗原表位
- N-Term
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适用
- 人, 马, 犬
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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 HGSNAT antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- RALAALLLAA SVLSAALLAP GGSSGRDAQA APPRDLDKKR HAELKMDQAL
- 预测反应
- Dog: 86%, Horse: 82%, Human: 100%
- 产品特性
- This is a rabbit polyclonal antibody against HGSNAT. It was validated on Western Blot.
- 纯化方法
- Affinity Purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the N-terminal region of Human HGSNAT
- Top Product
- Discover our top product HGSNAT Primary Antibody
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anti-Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT) (C-Term) antibody
HGSNAT 适用: 人, 小鼠, 马, 犬, 豚鼠, 兔, 大鼠, Cow WB 宿主: 兔 Polyclonal unconjugated
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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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- 抗原
- HGSNAT (Heparan-alpha-Glucosaminide N-Acetyltransferase (HGSNAT))
- 别名
- HGSNAT (HGSNAT 产品)
- 别名
- 9430010M12Rik antibody, AW208455 antibody, D8Ertd354e antibody, Tmem76 antibody, HGNAT antibody, MPS3C antibody, TMEM76 antibody, T1G16.60 antibody, T1G16_60 antibody, RGD1560755 antibody, heparan-alpha-glucosaminide N-acetyltransferase antibody, heparan-alpha-glucosaminide N-acetyltransferase-like protein (DUF1624) antibody, heparan-alpha-glucosaminide n-acetyltransferase antibody, Heparan-alpha-glucosaminide N-acetyltransferase antibody, Hgsnat antibody, HGSNAT antibody, hgsnat antibody, AT5G27730 antibody, Celal_1346 antibody, Celly_1273 antibody, Mahau_2889 antibody
- 背景
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This gene encodes a lysosomal acetyltransferase, which is one of several enzymes involved in the lysosomal degradation of heparin sulfate. Mutations in this gene are associated with Sanfilippo syndrome C, one type of the lysosomal storage disease mucopolysaccaridosis III, which results from impaired degradation of heparan sulfate.
Protein Size: 219 - 分子量
- 24 kDa
- 基因ID
- 138050
- UniProt
- Q8IVU6
- 途径
- Glycosaminoglycan Metabolic Process
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