中文名稱：兔抗TNNT1多克隆抗體

英文名稱： Anti-TNNT1 rabbit polyclonal antibody

別名： troponin T1, slow skeletal type; ANM; TNT; NEM5; STNT; TNTS

相關(guān)類別：一抗

儲(chǔ) 存： 冷凍（-20℃）

宿主： Rabbit

抗原： TNNT1

反應(yīng)種屬： Human

標(biāo) 記物： Unconjugate

克隆類型： rabbit polyclonal

技術(shù)規(guī)格

Background:

This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.

Applications:

ELISA, IHC

Name of antibody:

TNNT1

Immunogen:

Fusion protein of human TNNT1

Full name:

troponin T1, slow skeletal type

Synonyms:

ANM; TNT; NEM5; STNT; TNTS

SwissProt:

P13805

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human liver cancer

IHC Recommend dilution:

50-200

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兔抗TNNT1多克隆抗體說(shuō)明書
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ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測(cè)試劑盒

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)胞專用培養(yǎng)基

細(xì)胞系

菌株

生化試劑

病理染色液

科研抗體

標(biāo)準(zhǔn)品

血清

形態(tài)病理檢測(cè)

分子病理

超微病理

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兔抗TNNT1多克隆抗體

Background:	This gene encodes a protein that is a subunit of troponin, which is a regulatory complex located on the thin filament of the sarcomere. This complex regulates striated muscle contraction in response to fluctuations in intracellular calcium concentration. This complex is composed of three subunits: troponin C, which binds calcium, troponin T, which binds tropomyosin, and troponin I, which is an inhibitory subunit. This protein is the slow skeletal troponin T subunit. Mutations in this gene cause nemaline myopathy type 5, also known as Amish nemaline myopathy, a neuromuscular disorder characterized by muscle weakness and rod-shaped, or nemaline, inclusions in skeletal muscle fibers which affects infants, resulting in death due to respiratory insufficiency, usually in the second year. Multiple transcript variants encoding different isoforms have been found for this gene.
Applications:	ELISA, IHC
Name of antibody:	TNNT1
Immunogen:	Fusion protein of human TNNT1
Full name:	troponin T1, slow skeletal type
Synonyms:	ANM; TNT; NEM5; STNT; TNTS
SwissProt:	P13805
ELISA Recommended dilution:	5000-10000
IHC positive control:	Human liver cancer
IHC Recommend dilution:	50-200