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中文名稱: 兔抗SPINK7多克隆抗體

英文名稱: Anti-SPINK7 rabbit polyclonal antibody

別名: ECG2; ECRG2

抗原: SPINK7

儲存: 冷凍（-20℃）

宿主: Rabbit

相關(guān)類別: 一抗

反應(yīng)種屬: Human

標(biāo) 記物: Unconjugate

克隆類型: rabbit polyclonal

技術(shù)規(guī)格

Background:

SPINK7 (serine peptidase inhibitor, Kazal type 7), also known as Ecg2 (esophagus cancer-related gene 2 protein), is a 76 amino acid secreted protein. Containing one Kazal-like domain, SPINK7 is thought to be a serine protease inhibitor. The gene that encodes SPINK7 maps to human chromosome 5, which contains 181 million base pairs encoding around 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.Probable serine protease inhibitor.

Applications:

ELISA, IHC

Name of antibody:

SPINK7

Immunogen:

Synthetic peptide of human SPINK7

Full name:

serine peptidase inhibitor, Kazal type 7 (putative)

Synonyms：

ECG2; ECRG2

SwissProt:

P58062

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human prostate cancer and Human lung cancer

IHC Recommend dilution:

25-100

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菌株

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兔抗SPINK7多克隆抗體

Background:	SPINK7 (serine peptidase inhibitor, Kazal type 7), also known as Ecg2 (esophagus cancer-related gene 2 protein), is a 76 amino acid secreted protein. Containing one Kazal-like domain, SPINK7 is thought to be a serine protease inhibitor. The gene that encodes SPINK7 maps to human chromosome 5, which contains 181 million base pairs encoding around 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.Probable serine protease inhibitor.
Applications:	ELISA, IHC
Name of antibody:	SPINK7
Immunogen:	Synthetic peptide of human SPINK7
Full name:	serine peptidase inhibitor, Kazal type 7 (putative)
Synonyms：	ECG2; ECRG2
SwissProt:	P58062
ELISA Recommended dilution:	2000-5000
IHC positive control:	Human prostate cancer and Human lung cancer
IHC Recommend dilution:	25-100