中文名稱(chēng)：兔抗DYSF多克隆抗體

英文名稱(chēng)： Anti-DYSF rabbit polyclonal antibody

別名： MMD1; FER1L1; LGMD2B

相關(guān)類(lèi)別： 一抗

儲(chǔ) 存： 冷凍（-20℃）

宿主： Rabbit

抗原： DYSF

反應(yīng)種屬： Human, Mouse

標(biāo) 記物： Unconjugate

克隆類(lèi)型： rabbit polyclonal

技術(shù)規(guī)格

Background:

The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants.

Applications:

ELISA, IHC

Name of antibody:

DYSF

Immunogen:

Synthetic peptide of human DYSF

Full name:

dysferlin

Synonyms：

MMD1; FER1L1; LGMD2B

SwissProt:

O75923

ELISA Recommended dilution:

2000-5000

IHC positive control:

Human brain

IHC Recommend dilution:

25-100

展開(kāi)全部

兔抗DYSF多克隆抗體說(shuō)明書(shū)
下載

欧美一级免费-欧美一级免费观看-欧美一级免费看-欧美一级免费片-jizzjizz大全-jizzjizz国产精品

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

細(xì)胞系

細(xì)胞庫(kù)

基礎(chǔ)培養(yǎng)基

完全培養(yǎng)基

原代細(xì)胞

細(xì)胞專(zhuān)用培養(yǎng)基

菌株

生化試劑

病理染色液

科研抗體

標(biāo)準(zhǔn)品

血清

產(chǎn)品中心

最新產(chǎn)品

相關(guān)文章

兔抗DYSF多克隆抗體

Background:	The protein encoded by this gene belongs to the ferlin family and is a skeletal muscle protein found associated with the sarcolemma. It is involved in muscle contraction and contains C2 domains that play a role in calcium-mediated membrane fusion events, suggesting that it may be involved in membrane regeneration and repair. In addition, the protein encoded by this gene binds caveolin-3, a skeletal muscle membrane protein which is important in the formation of caveolae. Specific mutations in this gene have been shown to cause autosomal recessive limb girdle muscular dystrophy type 2B (LGMD2B) as well as Miyoshi myopathy. Alternative splicing results in multiple transcript variants.
Applications:	ELISA, IHC
Name of antibody:	DYSF
Immunogen:	Synthetic peptide of human DYSF
Full name:	dysferlin
Synonyms：	MMD1; FER1L1; LGMD2B
SwissProt:	O75923
ELISA Recommended dilution:	2000-5000
IHC positive control:	Human brain
IHC Recommend dilution:	25-100