Galactosidase, alpha (GLA) Peptide
GLA
适用: 人
宿主: 合成
BP, WB
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- 抗原 See all GLA products
- GLA (Galactosidase, alpha (GLA))
- 宿主
- 人
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资源
- 合成
- 应用范围
- Blocking Peptide (BP), Western Blotting (WB)
- 产品特性
- This is a synthetic peptide designed for use in combination with anti-GLA antibody (Catalog #: ARP54296_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- 纯化方法
- Purified
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- 应用备注
- Each Investigator should determine their own optimal working dilution for specific applications.
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- 浓度
- 1 mg/mL
- 缓冲液
- Final peptide concentration is 1 mg/mL in PBS.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- 抗原
- GLA (Galactosidase, alpha (GLA))
- 别名
- GALA Peptide, Ags Peptide, zgc:101584 Peptide, MGC130872 Peptide, SMU.877 Peptide, SCF11.21 Peptide, AO090005000217 Peptide, alpha-GAL Peptide, galactosidase alpha Peptide, galactosidase, alpha Peptide, galactosidase alpha S homeolog Peptide, alpha-galactosidase Peptide, aga Peptide, alpha-galactosidase A Peptide, GLA Peptide, Gla Peptide, gla Peptide, gla.S Peptide, agaN Peptide, aga Peptide, agaL Peptide, SCO0541 Peptide, rafA Peptide, melA Peptide, galA Peptide, ANI_1_2528074 Peptide, ANI_1_1502124 Peptide, AOR_1_390174 Peptide, CpipJ_CPIJ002066 Peptide, MCYG_00962 Peptide, MCYG_00791 Peptide, Tsp_02909 Peptide, Tsp_02508 Peptide
- 背景
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GLA is a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: GALA
Protein Interaction Partner: GLA,OTUD4
Protein Size: 429 - 分子量
- 45 kDa
- 基因ID
- 2717
- NCBI登录号
- NM_000169, NP_000160
- UniProt
- P06280
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