GBA 抗体
(Glucosidase, Beta, Acid (GBA))
This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010].
| Catalog no. | 产品 | 适用 | 宿主 / 克隆类型 | 应用 | 价格和交货时间 |
|---|---|---|---|---|---|
| Recombinant GBA 抗体 (Biotin) | 人, 大鼠 | 兔 Monoclonal |
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| Recombinant GBA 抗体 (Alexa Fluor 647) | 人, 大鼠 | 兔 Monoclonal |
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| Recombinant GBA 抗体 (Alexa Fluor 594) | 人, 大鼠 | 兔 Monoclonal |
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| Recombinant GBA 抗体 (Alexa Fluor 488) | 人, 大鼠 | 兔 Monoclonal |
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| GBA 抗体 (Center) | 人 | 小鼠 Monoclonal |
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| GBA 抗体 | 人 | 兔 Monoclonal |
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| GBA 抗体 | 人 | 小鼠 Monoclonal |
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| GBA 抗体 | 人, 小鼠 | 兔 Polyclonal |
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| GBA 抗体 (AA 337-365) | 人, 小鼠 | 兔 Polyclonal |
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| GBA 抗体 (N-Term) | 人, 小鼠, 大鼠, 犬, Pig, Cow, 豚鼠, 马, 兔 | 兔 Polyclonal |
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Primary Antibody
- 适用
- 人, 大鼠
- 宿主
- 兔
- 克隆形成能力
- Monoclonal
- 标记
- Biotin
- 蛋白类型
- Recombinant Antibody
Primary Antibody
- 适用
- 人, 大鼠
- 宿主
- 兔
- 克隆形成能力
- Monoclonal
- 标记
- Alexa Fluor 647
- 蛋白类型
- Recombinant Antibody
Primary Antibody
- 适用
- 人, 大鼠
- 宿主
- 兔
- 克隆形成能力
- Monoclonal
- 标记
- Alexa Fluor 594
- 蛋白类型
- Recombinant Antibody
Primary Antibody
- 适用
- 人, 大鼠
- 宿主
- 兔
- 克隆形成能力
- Monoclonal
- 标记
- Alexa Fluor 488
- 蛋白类型
- Recombinant Antibody
Primary Antibody
- WB (Western Blotting: 所列应用)
- 适用
- 人
- 宿主
- 小鼠
- 克隆形成能力
- Monoclonal
- 标记
- unconjugated
- 抗原表位
- Center
Primary Antibody
- WB (Western Blotting: 所列应用)
- IHC (p) (Immunohistochemistry (Paraffin-embedded Sections): 所列应用)
- FACS (Flow Cytometry: 所列应用)
- 适用
- 人, 小鼠
- 宿主
- 兔
- 克隆形成能力
- Polyclonal
- 标记
- unconjugated
- 抗体亚型
- IgG
- 抗原表位
- AA 337-365
Primary Antibody
- WB (Western Blotting: 所列应用)
- 适用
- 人, 小鼠, 大鼠, 犬, Pig, Cow, 豚鼠, 马, 兔
- 宿主
- 兔
- 克隆形成能力
- Polyclonal
- 标记
- unconjugated
- 抗原表位
- N-Term
Latest Publications for our GBA 抗体
: "LRRK2 modifies α-syn pathology and spread in mouse models and human neurons." in: Acta neuropathologica, Vol. 137, Issue 6, pp. 961-980, (2019) (PubMed).
: "Fetal gene therapy for neurodegenerative disease of infants." in: Nature medicine, Vol. 24, Issue 9, pp. 1317-1323, (2018) (PubMed).
: "Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling." in: Human molecular genetics, Vol. 24, Issue 5, pp. 1280-94, (2015) (PubMed).
: "Reduced glucocerebrosidase is associated with increased ?-synuclein in sporadic Parkinson's disease." in: Brain : a journal of neurology, Vol. 137, Issue Pt 3, pp. 834-48, (2014) (PubMed).
: "Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS." in: Orphanet journal of rare diseases, Vol. 9, pp. 86, (2014) (PubMed).
: "Gaucher disease paradigm: from ERAD to comorbidity." in: Human mutation, Vol. 33, Issue 10, pp. 1398-407, (2012) (PubMed).
: "Characterization of the ERAD process of the L444P mutant glucocerebrosidase variant." in: Blood cells, molecules & diseases, Vol. 46, Issue 1, pp. 4-10, (2011) (PubMed).
: "Characterization of Gaucher disease bone marrow mesenchymal stromal cells reveals an altered inflammatory secretome." in: Blood, Vol. 114, Issue 15, pp. 3181-90, (2009) (PubMed).
: "Fetal gene therapy for neurodegenerative disease of infants." in: Nature medicine, Vol. 24, Issue 9, pp. 1317-1323, (2018) (PubMed).
: "Glucocerebrosidase deficiency in zebrafish affects primary bone ossification through increased oxidative stress and reduced Wnt/β-catenin signaling." in: Human molecular genetics, Vol. 24, Issue 5, pp. 1280-94, (2015) (PubMed).
: "Reduced glucocerebrosidase is associated with increased ?-synuclein in sporadic Parkinson's disease." in: Brain : a journal of neurology, Vol. 137, Issue Pt 3, pp. 834-48, (2014) (PubMed).
: "Parkin-mediated ubiquitination of mutant glucocerebrosidase leads to competition with its substrates PARIS and ARTS." in: Orphanet journal of rare diseases, Vol. 9, pp. 86, (2014) (PubMed).
: "Gaucher disease paradigm: from ERAD to comorbidity." in: Human mutation, Vol. 33, Issue 10, pp. 1398-407, (2012) (PubMed).
: "Characterization of the ERAD process of the L444P mutant glucocerebrosidase variant." in: Blood cells, molecules & diseases, Vol. 46, Issue 1, pp. 4-10, (2011) (PubMed).
: "Characterization of Gaucher disease bone marrow mesenchymal stromal cells reveals an altered inflammatory secretome." in: Blood, Vol. 114, Issue 15, pp. 3181-90, (2009) (PubMed).
Aliases for GBA 抗体
glucosylceramidase beta (GBA) 抗体beta glucosidase 25 (BGLU25) 抗体
beta-glucosidase (PSPTO_3318) 抗体
beta-glucosidase (bglX) 抗体
Beta-glucosidase (bglA4) 抗体
glucosidase, beta, acid (Gba) 抗体
glucosylceramidase beta (Gba) 抗体
glucosylceramidase (LOC100399524) 抗体
beta-glucosidase (bglA.2) 抗体
bglX-2 (bglX-2) 抗体
glucosidase, beta, acid (GBA) 抗体
BETA-GLUCOSIDASE 抗体
betaGC 抗体
beta glucosidase 25 抗体
GBA1 抗体
GC 抗体
GCase 抗体
GCB 抗体
GLUC 抗体
PSPTO3318 抗体
PSPTO4290 抗体
T12J13.8 抗体
T12J13_8 抗体
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