Invitrogen

PAH Polyclonal Antibody

Name: PAH Polyclonal Antibody
Brand: Invitrogen
SKU: PA5-55840

高级验证

查看其他16个PAH抗体

说明书

实验方案

问题与答案

技术支持

说明书

实验方案

问题与答案

技术支持

抗体检测数据 (7)
高级验证 (2)

PAH Antibody in Immunohistochemistry (IHC)

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PAH Antibody (PA5-55840) in IHC

Immunohistochemical staining of PAH in human cerebral cortex, gallbladder, kidney and liver using PAH Polyclonal Antibody (Product # PA5-55840) (A) shows similar protein distribution across tissues to an independent PAH Polyclonal Antibody (B).

Product Image Gallery

PAH Antibody — Relative expression in different tissues in IHC: Detection of differential expression levels of PAH demonstrates antibody specificity. Immunohistochemical analysis of PAH using anti-PAH Polyclonal Antibody (Product # PA5-55840), shows significant staining of PAH in human liver and shows minimal or weak staining in human pancreas tissues. The relative expression levels of PAH within each tissue is shown using RNA-Seq. {RE}

Immunogen image

Immunogen Image PAH Polyclonal Antibody

产品信息

PA5-55840

应用

建议稀释比

已发表文章

免疫印迹 (WB)

0.04-0.4 µg/mL

免疫组化（石蜡） (IHC (P))

1:500-1:1,000

产品规格

种属反应

Human

宿主/亚型

Rabbit / IgG

分类

Polyclonal

类型

Antibody

抗原

Recombinant protein corresponding to Human PAH. Recombinant protein control fragment (Product #RP-99363).

查看免疫原

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

0.1 mg/mL

纯化类型

Antigen affinity chromatography

保存液

PBS, pH 7.2, with 40% glycerol

内含物

0.02% sodium azide

保存条件

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

运输条件

Ambient (domestic); Wet ice (international)

AB_2645174

产品详细信息

Immunogen sequence: MSTAVLENPG LGRKLSDFGQ ETSYIEDNCN QNGAISLIFS LKEEVGALAK VLRLFEENDV NLTHIESRPS RLKKDEYEFF THLDKRSLPA LTNIIKILRH DIGATVHELS RDKKKDTVPW FPRTIQELDR FANQILSYGA ELDADHPG

Highest antigen sequence identity to the following orthologs: Mouse - 86%, Rat - 88%.

靶标信息

PAH encodes the enzyme phenylalanine hydroxylase that is the rate-limiting step in phenylalanine catabolism. Deficiency of this enzyme activity results in the autosomal recessive disorder phenylketonuria.

仅用于科研。不用于诊断过程。未经明确授权不得转售。