中文名稱：兔抗SNX29多克隆抗體

英文名稱： Anti-SNX29 rabbit polyclonal antibody

別名： RUNDC2A; A-388D4.1

相關(guān)類別：一抗

儲(chǔ) 存： 冷凍（-20℃）

宿主： Rabbit

抗原： SNX29

反應(yīng)種屬： Human, Mouse

標(biāo) 記物： Unconjugate

克隆類型： rabbit polyclonal

技術(shù)規(guī)格

Background:

SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Applications:

ELISA, IHC

Name of antibody:

SNX29

Immunogen:

Synthetic peptide of human SNX29

Full name:

sorting nexin 29

Synonyms：

RUNDC2A; A-388D4.1

SwissProt:

Q8TEQ0

ELISA Recommended dilution:

1000-2000

IHC positive control:

Human liver cancer and Human colon cancer

IHC Recommend dilution:

25-100

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兔抗SNX29多克隆抗體

Background:	SNX29 also known as RUNDC2A, is a 375 amino protein that contains one RUN domain. RUNDC2A is encoded by a gene that maps to human chromosome 16p13.13, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
Applications:	ELISA, IHC
Name of antibody:	SNX29
Immunogen:	Synthetic peptide of human SNX29
Full name:	sorting nexin 29
Synonyms：	RUNDC2A; A-388D4.1
SwissProt:	Q8TEQ0
ELISA Recommended dilution:	1000-2000
IHC positive control:	Human liver cancer and Human colon cancer
IHC Recommend dilution:	25-100