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GLA 抗体 (N-Term)

Name: GLA 抗体 (N-Term)
SKU: ABIN453055
Availability: OutOfStock

GLA 适用: 人 WB, EIA 宿主: 兔 Polyclonal unconjugated

Western blot analysis of GLA antibody (N-term) in Hela cell line lysates (35 µg/lane).

GLA Antibody (N-term) IHC analysis in formalin fixed and paraffin embedded human Lung carcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining.

IHC (p)

2 images

产品编号 ABIN453055

发货至: 中国

Datasheet as PDF

抗原 See all GLA 抗体

GLA (Galactosidase, alpha (GLA))
抗原表位
16

5

5

4

4

4

4

3

3

2

2

2

1

1

1
AA 90-120, N-Term
适用
55

30

20

4

4

4

2

2

2

1

1

1

1

1

1
人
宿主
66

8

2
兔
Compatible Secondaries
克隆类型
70

6
多克隆
标记
32

13

12

7

1

1

1

1

1

1

1

1

1

1

1

1
This GLA antibody is un-conjugated
应用范围
62

34

17

17

13

13

8

7

6

6

4

3

3
Western Blotting (WB), Enzyme Immunoassay (EIA)

特异性

This antibody detects GLA at N-term.

纯化方法

Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS

免疫原

KLH conjugated synthetic peptide between 90~120 amino acids from the N-terminal region of human GLA

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应用备注

Western blot: 1: 50 - 1: 100. ELISA: 1: 1,000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

限制

仅限研究用
状态

Liquid

浓度

0.25 mg/mL

缓冲液

PBS with 0.09 % (W/V) sodium azide as preservative

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 repeated freezing and thawing.

储存条件

4 °C/-20 °C

储存方法

Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer.
抗原

GLA (Galactosidase, alpha (GLA))

别名

alpha-Galactosidase A (GLA 产品)

背景

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.Synonyms: Alpha-D-galactosidase A, Alpha-D-galactoside galactohydrolase, GLA, Melibiase

分子量

48767 Da

基因ID

2717

NCBI登录号

NP_000160

UniProt

P06280

途径

SARS-CoV-2 Protein Interactome