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CDKN3 rabbit Polyclonal Antibody

CDKN3抗体
CDKN3抗体应用:WB 1:500-2000, ELISA 1:10000-20000 cyclin dependent kinase inhibitor 3(CDKN3) Homo sapiens The protein encoded by this gene belongs to the dual specificity protein phosphatase family. It was identified as a cyclin-dependent kinase inhibitor, and has been shown to interact with, and dephosphorylate CDK2 kinase, thus prevent the activation of CDK2 kinase. This gene was reported to be deleted, mutated, or overexpressed in several kinds of cancers. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008],

CDNF rabbit Polyclonal Antibody

CDNF抗体
CDNF抗体应用:IHC-p 1:50-200, ELISA 1:10000-20000 CDNF (Cerebral Dopamine Neurotrophic Factor) is a Protein Coding gene. Trophic factor for dopamine neurons. Prevents the 6-hydroxydopamine (6-OHDA)-induced degeneration of dopaminergic neurons. When administered after 6-OHDA-lesioning, restores the dopaminergic function and prevents the degeneration of dopaminergic neurons in substantia nigra (By similarity).

CDO rabbit Polyclonal Antibody

CDO抗体
CDO抗体应用:Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. cell adhesion associated, oncogene regulated(CDON) Homo sapiens This gene encodes a cell surface receptor that is a member of the immunoglobulin superfamily. The encoded protein contains three fibronectin type III domains and five immunoglobulin-like C2-type domains. This protein is a member of a cell-surface receptor complex that mediates cell-cell interactions between muscle precursor cells and positively regulates myogenesis. [provided by RefSeq, Aug 2011],

CDR2 rabbit Polyclonal Antibody

CDR2抗体
CDR2抗体应用:WB 1:500-2000

Cdx2 rabbit Polyclonal Antibody

Cdx2抗体
Cdx2抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/5000. caudal type homeobox 2(CDX2) Homo sapiens This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded protein is a major regulator of intestine-specific genes involved in cell growth an differentiation. This protein also plays a role in early embryonic development of the intestinal tract. Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis. [provided by RefSeq, Jan 2012],

Cdx2 rabbit Polyclonal Antibody

Cdx2抗体
Cdx2抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/5000. caudal type homeobox 2(CDX2) Homo sapiens This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded protein is a major regulator of intestine-specific genes involved in cell growth an differentiation. This protein also plays a role in early embryonic development of the intestinal tract. Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis. [provided by RefSeq, Jan 2012], 相关产品

Cdx2 rabbit Polyclonal Antibody

Cdx2抗体
Cdx2抗体应用:WB 1:500-2000, ELISA 1:10000-20000 caudal type homeobox 2(CDX2) Homo sapiens This gene is a member of the caudal-related homeobox transcription factor gene family. The encoded protein is a major regulator of intestine-specific genes involved in cell growth an differentiation. This protein also plays a role in early embryonic development of the intestinal tract. Aberrant expression of this gene is associated with intestinal inflammation and tumorigenesis. [provided by RefSeq, Jan 2012],

CDYL2 rabbit Polyclonal Antibody

CDYL2抗体
CDYL2抗体应用:Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunocytochemistry: 1/200 - 1/1000. ELISA: 1/20000. similarity:Contains 1 chromo domain.,tissue specificity:Ubiquitously expressed.,

CE046 rabbit Polyclonal Antibody

CE046抗体
CE046抗体应用:IHC-p 1:50-200

CE120 rabbit Polyclonal Antibody

CE120抗体
CE120抗体应用:WB 1:500-2000 This gene encodes a protein that functions in the microtubule-dependent coupling of the nucleus and the centrosome. A similar protein in mouse plays a role in both interkinetic nuclear migration, which is a characteristic pattern of nuclear movement in neural progenitors, and in neural progenitor self-renewal. Mutations in this gene are predicted to result in neurogenic defects. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009],
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