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抗體

ACL Polyclonal Antibody

Polyclonal抗體
ACL Polyclonal AntibodyWB: 1:500-1:2000; IHC:1:20-1:200;ELISA:1:1000-1:5000

ACSS2 Polyclonal Antibody

Polyclonal抗體
ACSS2 Polyclonal Antibody

Actinin Polyclonal Antibody

Actinin抗體
Actinin Polyclonal AntibodyWB: 1:500-1:2000; IHC:1:20-1:200;ELISA:1:1000-1:5000

ADAM/TACE Polyclonal Antibody

ADAM/TACE抗體
ADAM/TACE Polyclonal AntibodyWB: 1:500-1:2000; IHC:1:20-1:200;ELISA:1:1000-1:5000

Anti NRP1 polyclonal antibody

NRP1抗體
Anti NRP1 polyclonal antibodyNeuropilin-1 (NRP1) is a a 130–140 kDa transmembrane glycoprotein expressed by endothelial, dendritic, and regulatory T cells, as well as several other normal cell types and malignant tumor cells. NRP1 was first identified as a semaphorin (SEMA) receptor, involved in axonal guidance in embryonic development. NRP1 was also shown to act as a receptor for vascular endothelial growth factor (VEGF) and a promoter of angiogenesis through its interaction with VEGF-A165 (and other VEGFs) and the receptor tyrosine kinase (RTK) VEGF-R2. NRP1 plays versatile roles in angiogenesis, axon guidance, cell survival, migration, and invasion.

Anti MAPK9 polyclonal antibody

MAPK9抗體
Anti MAPK9 polyclonal antibodyThe protein encoded by this gene is a member of the MAP kinase family. MAP kinases act as an integration point for multiple biochemical signals, and are involved in a wide variety of cellular processes such as proliferation, differentiation, transcription regulation and development. This kinase targets specific transcription factors, and thus mediates immediate-early gene expression in response to various cell stimuli. It is most closely related to MAPK8, both of which are involved in UV radiation induced apoptosis, thought to be related to the cytochrome c-mediated cell death pathway. This gene and MAPK8 are also known as c-Jun N-terminal kinases. This kinase blocks the ubiquitination of tumor suppressor p53, and thus it increases the stability of p53 in nonstressed cells. Studies of this gene's mouse counterpart suggest a key role in T-cell differentiation. Several alternatively spliced transcript variants encoding distinct isoforms have been reported. [

Anti REG1b polyclonal antibody

REG1b抗體
Anti REG1b polyclonal antibodyReg protein is stimulated during the regeneration of pancreatic islets. In human, there are four REG family genes,REG 1 alpha, REG 1 beta, REG-related sequence (RS) and HIP/PAP. These Reg-related proteins are classified into four subfamilies according to their amino-acid sequences, but they share a similar structure and physiological function.

Anti Ki67 polyclonal antibody

Ki67抗體
Anti Ki67 polyclonal antibodyThe Ki-67 protein (also known as MKI67) is a cellular marker for proliferation. Ki67 is present during all active phases of the cell cycle (G1, S, G2 and M), but is absent in resting cells (G0). Cellular content of Ki-67 protein markedly increases during cell progression through S phase of the cell cycle. Therefore, the nuclear expression of Ki67 can be evaluated to assess tumor proliferation by immunohistochemistry. It has been demonstrated to be of prognostic value in breast cancer. In head and neck cancer, several studies have reported an association between high proliferative activity and poorer prognosis.

Anti CD71 polyclonal antibody

CD71抗體
Anti CD71 polyclonal antibodyCD71, also known as transferrin receptor protein 1 (TfR1), is a transmembrane glycoprotein composed of two disulfide-linked monomers, each of 90 kDa molecular weight. Each monomer binds one holo-transferrin molecule creating an iron-Tf-TfR complex which enters the cell by endocytosis. CD71 is present on actively proliferating cells and is essential for iron transport into proliferating cells.

icon Anti CX43 polyclonal antibody

CX43抗體
Anti CX43 polyclonal antibodyConnexin-43 (Cx43, also known as gap junction alpha-1), a member of connexin family, plays essential roles in gap junction communication that facilitates direct communication among adjacent cells (PMID: 12270943). Usually, six connexin proteins oligomerize into a hemi-channel or connexon during intercellular channel formation (PMID: 12270943). Mutations of Cx43 may cause a series of diseases such as oculodentodigital dysplasia (ODDD), syndactyly 3 (SDTY3), hypoplastic left heart syndrome 1 (HLHS1) and so on (PMID: 18161618, 1472936, 1147490).
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