中文名稱：兔抗TBX1多克隆抗體

英文名稱： Anti-TBX1 rabbit polyclonal antibody

級別： DGS; TGA; VCF; CAFS; CTHM; DGCR; DORV; VCFS; TBX1C; CATCH22

抗原： TBX1

儲存： 冷凍（-20℃）

宿主： Rabbit

相關類別：一抗

反應種屬： Human

標記物： Unconjugate

克隆類型： rabbit polyclonal

技術規(guī)格

Background:

This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.

Applications:

ELISA, WB, IHC

Name of antibody:

TBX1

Immunogen:

Synthetic peptide of human TBX1

Full name:

T-box 1

Synonyms:

DGS; TGA; VCF; CAFS; CTHM; DGCR; DORV; VCFS; TBX1C; CATCH22

SwissProt:

O43435

ELISA Recommended dilution:

5000-10000

IHC positive control:

Human liver cancer

IHC Recommend dilution:

25-100

WB Predicted band size:

43 kDa

WB Positive control:

293T and Hela cell lysates

WB Recommended dilution:

500-2000

021-54845833/15800441009

ELISA試劑盒

PCR試劑盒

生化試劑盒

農(nóng)殘檢測試劑盒

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

細胞系

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

細胞凋亡與檢測

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相關文章

兔抗TBX1多克隆抗體

Background:	This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98% amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.
Applications:	ELISA, WB, IHC
Name of antibody:	TBX1
Immunogen:	Synthetic peptide of human TBX1
Full name:	T-box 1
Synonyms:	DGS; TGA; VCF; CAFS; CTHM; DGCR; DORV; VCFS; TBX1C; CATCH22
SwissProt:	O43435
ELISA Recommended dilution:	5000-10000
IHC positive control:	Human liver cancer
IHC Recommend dilution:	25-100
WB Predicted band size:	43 kDa
WB Positive control:	293T and Hela cell lysates
WB Recommended dilution:	500-2000