抗体

CCDC102B rabbit Polyclonal Antibody

CCDC102B抗体
CCDC102B抗体应用:Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. CCDC102B (coiled-coil domain containing 102B), also known as AN, ACY1L or HsT1731, is a 513 amino acid protein that exists as three alternatively spliced isoforms. Widely expressed and found in multiple CNV (copy-number variant) regions, CCDC102B contains the deletion breakpoint of a maternally inherited deletion, which is 2.7 Mb in size, and maps to human chromosome 18q22.1. CCDC102B may play a role in the pathogenesis of diaphragmatic hernia, microphthalmia, colorectal carcinoma and schizophrenia. Encoding over 300 genes, chromosome 18 contains about 76 million bases. Translocation between chromosomes 18 and 14 is the most common translocation in cancers and occurs in follicular lymphomas. Niemann-Pick disease, hereditary hemorrhagic telangiectasia and erythropoietic protoporphyria are associated with chromosome 18.

CCDC109A rabbit Polyclonal Antibody

CCDC109A抗体
CCDC109A抗体应用:Immunohistochemistry: 1/100 - 1/300. ELISA: 1/40000. mitochondrial calcium uniporter(MCU) Homo sapiens This gene encodes a calcium transporter that localizes to the mitochondrial inner membrane. The encoded protein interacts with mitochondrial calcium uptake 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012],

CCDC4 rabbit Polyclonal Antibody

CCDC4抗体
CCDC4抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/40000. PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,similarity:Contains 1 BEN domain.,

CCDC45 rabbit Polyclonal Antibody

CCDC45抗体
CCDC45抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/40000. PTM:Phosphorylated upon DNA damage, probably by ATM or ATR.,

CCDC7 rabbit Polyclonal Antibody

CCDC7抗体
CCDC7抗体应用:WB 1:500-2000

CCDC99 rabbit Polyclonal Antibody

CCDC99抗体
CCDC99抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/40000. spindle apparatus coiled-coil protein 1(SPDL1) Homo sapiens This gene encodes a coiled-coil domain-containing protein that functions in mitotic spindle formation and chromosome segregation. The encoded protein plays a role in coordinating microtubule attachment by promoting recruitment of dynein proteins, and in mitotic checkpoint signaling. [provided by RefSeq, Jul 2016],

CCHCR rabbit Polyclonal Antibody

CCHCR抗体
CCHCR抗体应用:WB 1:500-2000

CCK rabbit Polyclonal Antibody

CCK抗体
CCK抗体应用:Immunohistochemistry: 1/100 - 1/300. ELISA: 1/20000. cholecystokinin(CCK) Homo sapiens This gene encodes a member of the gastrin/cholecystokinin family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including the peptide hormones cholecystokinin-8, -12, -33, and others. The encoded peptides have been shown to regulate gastric acid secretion and food intake. A sulfated form of cholecystokinin-8 may modulate neuronal activity in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2015],

CCK-AR rabbit Polyclonal Antibody

CCK-AR抗体
CCK-AR抗体应用:Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. cholecystokinin A receptor(CCKAR) Homo sapiens This gene encodes a G-protein coupled receptor that binds non-sulfated members of the cholecystokinin (CCK) family of peptide hormones. This receptor is a major physiologic mediator of pancreatic enzyme secretion and smooth muscle contraction of the gallbladder and stomach. In the central and peripheral nervous system this receptor regulates satiety and the release of beta-endorphin and dopamine. [provided by RefSeq, Jul 2008],

CCK-BR rabbit Polyclonal Antibody

CCK-BR抗体
CCK-BR抗体应用:Western Blot: 1/500 - 1/2000. ELISA: 1/20000. cholecystokinin B receptor(CCKBR) Homo sapiens This gene encodes a G-protein coupled receptor for gastrin and cholecystokinin (CCK), regulatory peptides of the brain and gastrointestinal tract. This protein is a type B gastrin receptor, which has a high affinity for both sulfated and nonsulfated CCK analogs and is found principally in the central nervous system and the gastrointestinal tract. Alternative splicing results in multiple transcript variants. A misspliced transcript variant including an intron has been observed in cells from colorectal and pancreatic tumors. [provided by RefSeq, Dec 2015],
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