Invitrogen

SI Polyclonal Antibody

SI Antibody in Immunohistochemistry (IHC)

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SI Antibody (PA5-52871) in IHC

Immunohistochemical staining of SI in human small intestine and stomach tissues using SI Polyclonal Antibody (Product # PA5-52871). Corresponding SI RNA-seq data are presented for the same tissues.

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SI Antibody — Relative expression in different tissues in IHC: Detection of differential expression levels of SI demonstrates antibody specificity. Immunohistochemical analysis of SI using anti-SI Polyclonal Antibody (Product # PA5-52871), shows significant staining of SI in human small intestine and shows minimal or weak staining in human stomach tissues. The relative expression levels of SI within each tissue is shown using RNA-Seq. {RE}

产品信息

PA5-52871

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))

1:500-1:1000

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 SI. Recombinant protein control fragment (Product #RP-90016).

查看免疫原

偶联物

Unconjugated Unconjugated Unconjugated

形式

Liquid

浓度

0.20 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

Wet ice

AB_2647292

产品详细信息

Immunogen sequence: PAVDEISDST STPATTRVTT NPSDSGKCPN VLNDPVNVRI NCIPEQFPTE GICAQRGCCW RPWNDSLIPW CFFVDNHGYN VQDMTTTSIG VEAKLNRIPS PTLFGNDINS VLFTTQNQTP NRFRFKITDP NNRRYEVPHQ YV

Highest antigen sequence identity to the following orthologs: Mouse - 61%, Rat - 63%.

靶标信息

This gene encodes a sucrase-isomaltase enzyme that is expressed in the intestinal brush border. The encoded protein is synthesized as a precursor protein that is cleaved by pancreatic proteases into two enzymatic subunits sucrase and isomaltase. These two subunits heterodimerize to form the sucrose-isomaltase complex. This complex is essential for the digestion of dietary carbohydrates including starch, sucrose and isomaltose. Mutations in this gene are the cause of congenital sucrase-isomaltase deficiency.

仅用于科研。不用于诊断过程。未经明确授权不得转售。