Invitrogen

Arylsulfatase A Polyclonal Antibody

Name: Arylsulfatase A Polyclonal Antibody
Brand: Invitrogen
SKU: PA5-118848
Availability: InStock

查看其他18个ARSA抗体

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

说明书

Certificates

实验方案

问题与答案

技术支持

Additional Information:

抗体检测数据 (5)

Arylsulfatase A Antibody in Immunocytochemistry (ICC/IF)

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Arylsulfatase A Antibody (PA5-118848) in ICC/IF

Immunocytochemical analysis of Arylsulfatase A in Hela cells using a Arylsulfatase A polyclonal antibody (Product # PA5-118848). The samples were fixed with PFA and permeabilized in 0.1% Triton X-100,then blocked in 10% serum for 45 minutes at 25°C. Samples were then incubated with the primary antibody and mouse anti-beta tubulin antibody at a dilution of 1:200 for 1 hour at 37°C. An AlexaFluor594 conjugate... View More

Arylsulfatase A Antibody in Immunohistochemistry (Paraffin) (IHC (P))

Arylsulfatase A Antibody in Western Blot (WB)

Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.

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Immunogen image

Immunogen Image Arylsulfatase A Polyclonal Antibody

产品信息

PA5-118848

应用

建议稀释比

已发表文章

免疫印迹 (WB)

1:500-1:1,000

免疫组化（石蜡） (IHC (P))

1:50-1:200

免疫细胞化学 (ICC/IF)

1:100-1:500

产品规格

种属反应

Human, Mouse, Rat

宿主/亚型

Rabbit / IgG

分类

Polyclonal

类型

Antibody

抗原

A synthesized peptide derived from human ARSA(Accession P15289), corresponding to amino acid residues V258-G308.

3D表位/免疫原

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

1 mg/mL

100 µg

纯化类型

Affinity chromatography

保存液

PBS, pH 7.4, with 50% glycerol

内含物

0.02% sodium azide

保存条件

-20°C

运输条件

Ambient (domestic); Wet ice (international)

AB_2903348

产品详细信息

Antibody detects endogenous levels of total ARSA.

靶标信息

The protein encoded by this gene hydrolyzes cerebroside sulfate to cerebroside and sulfate. Defects in this gene lead to metachromatic leucodystrophy, a progressive demyelination disease which results in a variety of neurological symptoms and ultimately death. Alternatively spliced transcript variants have been described for this gene.

仅用于科研。不用于诊断过程。未经明确授权不得转售。