中文名稱：兔抗DTWD1多克隆抗體

英文名稱： Anti-DTWD1 rabbit polyclonal antibody

別名： MDS009

相關類別： 一抗

儲存： 冷凍（-20℃）

宿主： Rabbit

抗原： DTWD1

反應種屬： Human

標記物： Unconjugate

克隆類型： rabbit polyclonal

技術規(guī)格

Background:

Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.

Applications:

ELISA, IHC

Name of antibody:

DTWD1

Immunogen:

Full length fusion protein

Full name:

DTW domain containing 1

Synonyms：

MDS009

SwissProt:

Q8N5C7

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human thyroid cancer and human colorectal cancer

IHC Recommend dilution:

20-100

展開全部

兔抗DTWD1多克隆抗體說明書
下載

久久综合九九-久久综合九九亚洲一区-久久综合九色-久久综合九色欧美综合狠狠-久久综合九色婷婷97-久久综合九色综合8888

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

細胞系

細胞庫

基礎培養(yǎng)基

完全培養(yǎng)基

原代細胞

細胞專用培養(yǎng)基

菌株

生化試劑

病理染色液

科研抗體

標準品

血清

形態(tài)病理檢測

分子病理

超微病理

產(chǎn)品中心

最新產(chǎn)品

相關文章

兔抗DTWD1多克隆抗體

Background:	Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.
Applications:	ELISA, IHC
Name of antibody:	DTWD1
Immunogen:	Full length fusion protein
Full name:	DTW domain containing 1
Synonyms：	MDS009
SwissProt:	Q8N5C7
ELISA Recommended dilution:	5000-10000
IHC positive control:	Human thyroid cancer and human colorectal cancer
IHC Recommend dilution:	20-100