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Merck

G4046

Sigma-Aldrich

抗グルコセレブロシダーゼ ウサギ宿主抗体

enhanced validation

~1 mg/mL, affinity isolated antibody, buffered aqueous solution

別名:

抗β-グルコシダーゼ(Gluc)抗体, 抗D-グルコシル-N-アシルスフィンゴシングルコヒドロラーゼ抗体, 抗GBA1抗体, 抗GBA抗体, 抗グルコシルセラミダーゼ(Glcセラーゼ)抗体, 抗リソソームグルコセレブロシダーゼ抗体

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About This Item

UNSPSCコード:
12352203
NACRES:
NA.41

由来生物

rabbit

結合体

unconjugated

抗体製品の状態

affinity isolated antibody

抗体製品タイプ

primary antibodies

クローン

polyclonal

フォーム

buffered aqueous solution

分子量

antigen ~60 kDa

交差性

mouse, human, rat

強化検証

recombinant expression
Learn more about Antibody Enhanced Validation

濃度

~1 mg/mL

テクニック

western blot: 1-2 μg/mL using HEK-293T cell lysate expressing human glucocerebrosidase (GBA) or SH-SY-5Y cell lysate

UniProtアクセッション番号

輸送温度

dry ice

保管温度

−20°C

ターゲットの翻訳後修飾

unmodified

遺伝子情報

human ... GBA(2629)
mouse ... Gba(14466)

詳細

GBA1 (β-glucocerebrosidase) gene is mapped to human chromosome 1q21. It is a lysosomal enzyme and is widely expressed. The protein has domain I with three stranded anti?parallel βsheets, domain II with two β sheets making an immunoglobulin like domain and domain III with eight stranded β/α triosephosphate isomerase (TIM) barrel.

アプリケーション

Anti-Glucocerebrosidase antibody produced in rabbit has been used in western blotting and immunocytochemistry.
Anti-Glucocerebrosidase antibody produced in rabbit is suitable for immunoblotting at a working concentration of 1-2μg/mL using HEK-293T cell lysate expressing human glucocerebrosidase (GBA).

生物化学的/生理学的作用

GBA (glucosidase, beta, acid) gene encodes a protein that cleaves the β-glucosidic linkage of glycosylceramide (GlcCer), an intermediate in glycolipid metabolism. Mutations in the human GBA gene cause a reduction in the GBA activity and accumulation of GlcCer in lysosomes of cells of the reticuloendothelial system. This causes Gaucher disease (GD), an inherited lysosomal storage disorder, characterised by severe loss of neurons in the central nervous system, fetal onset, hydrops fetalis, in utero fetal death and neonatal distress. It leads to changes in neuronal functionality including increased levels of tubular endoplasmic reticulum (ER) elements, a large increase in Ca2+ release from the ER in response to glutamate, and an increased sensitivity to glutamate-induced neurotoxicity. Mutations in the human GBA gene may contribute to the development of common age-related dementia known as dementia with Lewy bodies or DLB and may cause early-onset of Parkinson disease.

物理的形状

0.01M PBS溶液 (pH 7.4, 15mMアジ化ナトリウム含有)。

免責事項

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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保管分類コード

12 - Non Combustible Liquids

WGK

WGK 1

引火点(°F)

Not applicable

引火点(℃)

Not applicable

個人用保護具 (PPE)

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

Jan Code

G4046-VAR:
G4046-200UL:
G4046-25UL:
G4046-BULK:


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試験成績書(COA)

Lot/Batch Number

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文書ライブラリで、最近購入した製品の文書を検索できます。

文書ライブラリにアクセスする

The relationship between glucocerebrosidase mutations and Parkinson disease
Migdalska RA, et al.
Journal of Neurochemistry, 1-1 (2016)
E Korkotian et al.
The Journal of biological chemistry, 274(31), 21673-21678 (1999-07-27)
Gaucher disease is a glycosphingolipid storage disease caused by defects in the activity of the lysosomal hydrolase, glucocerebrosidase (GlcCerase), resulting in accumulation of glucocerebroside (glucosylceramide, GlcCer) in lysosomes. The acute neuronopathic type of the disease is characterized by severe loss
K P Zimmer et al.
The Journal of pathology, 188(4), 407-414 (1999-08-10)
Gaucher's disease (GD) is caused by an inherited deficiency of acid beta-glucosidase with storage of glucosylceramides in the lysosomes of macrophages. This study identifies a G202R mutation in the acid beta-glucosidase gene in an infant with severe neuronopathic (type 2)
Dermal fibroblasts from patients with Parkinson?s disease have normal GCase activity and autophagy compared to patients with PD and GBA mutations
Collins LM, et al.
F1000Research (2017)
Individualized screening for chaperone activity in Gaucher disease using multiple patient derived primary cell lines
Ivanova MM, et al.
American Journal of Translational Research, 10(11), 3750-3750 (2018)

ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.

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