Invitrogen

SERPINB11 Polyclonal Antibody

Name: SERPINB11 Polyclonal Antibody
Brand: Invitrogen
SKU: PA5-50876
Availability: InStock

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 (2)

SERPINB11 Antibody in Immunohistochemistry (Paraffin) (IHC (P))

图: 1 / 2

SERPINB11 Antibody (PA5-50876) in IHC (P)

Immunohistochemical analysis of SERPINB11 in paraffin embedded Human thyroid cancer tissue using SERPINB11 Polyclonal Antibody (Product # PA5-50876) at a 1:100 dilution.

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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产品信息

PA5-50876

应用

建议稀释比

已发表文章

免疫印迹 (WB)

1:500-1:2,000

免疫组化（石蜡） (IHC (P))

1:100-1:200

产品规格

种属反应

Human, Mouse

宿主/亚型

Rabbit / IgG

分类

Polyclonal

类型

Antibody

抗原

Fusion protein of human serpin peptidase inhibitor, clade B (ovalbumin), member 11 (gene/pseudogene)

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

1.2 mg/mL

120 µg

纯化类型

Antigen affinity chromatography

保存液

PBS, pH 7.4, with 40% glycerol

内含物

0.05% sodium azide

保存条件

-20°C

运输条件

Ambient (domestic); Wet ice (international)

AB_2636328

产品详细信息

The antibody detects endogenous levels of total SERPINB11 protein.

靶标信息

SerpinB11 (serpin peptidase inhibitor, clade B (ovalbumin), member 11), also known as EPIPIN or SERPIN11, is a 392 amino acid cytoplasmic protein that belongs to the Ov-serpin subfamily and serpin family. Like other members of the serpin family, SerpinB11 has been identified as a noninhibitory intracellular protein. The gene encoding SerpinB11 maps to human chromosome 18, which houses over 300 protein-coding genes and contains nearly 76 million bases. There are a variety of diseases associated with defects in chromosome 18-localized genes, some of which include Trisomy 18 (also known as Edwards syndrome), Niemann-Pick disease, hereditary hemorrhagic telangiectasia, erythropoietic protoporphyria and follicular lymphomas.

仅用于科研。不用于诊断过程。未经明确授权不得转售。