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CRERF抗體應(yīng)用：WB 1:500-2000

CRGC抗體應(yīng)用：WB 1:500-2000This gene encodes a member of the beta/gamma-crystallin family of proteins. Crystallins constitute the major proteins of vertebrate eye lens and maintain the transparency and refractive index of the lens. This gene and several family members are present in a gene cluster on chromosome 2. Mutations in this gene have been shown to cause multiple types of cataract, including Coppock-like cataract and zonular pulverulent cataract, among others. [provided by RefSeq, Jan 2015],

CRHBP抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000corticotropin releasing hormone binding protein(CRHBP) Homo sapiens Corticotropin-releasing hormone is a potent stimulator of synthesis and secretion of preopiomelanocortin-derived peptides. Although CRH concentrations in the human peripheral circulation are normally low, they increase throughout pregnancy and fall rapidly after parturition. Maternal plasma CRH probably originates from the placenta. Human plasma contains a CRH-binding protein which inactivates CRH and which may prevent inappropriate pituitary-adrenal stimulation in pregnancy. [provided by RefSeq, Jul 2008],

CRIS2抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000function:May regulate some ion channels' activity and therebye regulate calcium fluxes during sperm capacitation.,similarity:Belongs to the CRISP family.,tissue specificity:Testis and epididymis.,

CRIS3抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000similarity:Belongs to the CRISP family.,subcellular location:In neutrophils, localized in specific granules.,tissue specificity:Salivary gland, pancreas and prostate > epididymis, ovary, thymus and colon.,

CRLF1抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000cytokine receptor like factor 1(CRLF1) Homo sapiens This gene encodes a member of the cytokine type I receptor family. The protein forms a secreted complex with cardiotrophin-like cytokine factor 1 and acts on cells expressing ciliary neurotrophic factor receptors. The complex can promote survival of neuronal cells. Mutations in this gene result in Crisponi syndrome and cold-induced sweating syndrome. [provided by RefSeq, Oct 2009],

CRLF2抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000cytokine receptor-like factor 2(CRLF2) Homo sapiens This gene encodes a member of the type I cytokine receptor family. The encoded protein is a receptor for thymic stromal lymphopoietin (TSLP). Together with the interleukin 7 receptor (IL7R), the encoded protein and TSLP activate STAT3, STAT5, and JAK2 pathways, which control processes such as cell proliferation and development of the hematopoietic system. Rearrangement of this gene with immunoglobulin heavy chain gene (IGH) on chromosome 14, or with P2Y purinoceptor 8 gene (P2RY8) on the same X or Y chromosomes is associated with B-progenitor acute lymphoblastic leukemia (ALL) and Down syndrome ALL. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2014],

CRLF3抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000cytokine receptor like factor 3(CRLF3) Homo sapiens This gene encodes a cytokine receptor-like factor that may negatively regulate cell cycle progression at the G0/G1 phase. Studies of the related rat protein suggest that it may regulate neuronal morphology and synaptic vesicle biogenesis. This gene is one of several genes located in the neurofibromatosis type I tumor suppressor region on the q arm of chromosome 17, a region that is subject to microdeletions, duplications, chromosomal breaks and rearrangements. Alternative splicing of this gene results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 2 and 5. [provided by RefSeq, Aug 2012],

CRLS1抗體應(yīng)用：WB 1:500-2000This gene encodes a member of the CDP-alcohol phosphatidyltransferase class-I family of proteins. The encoded enzyme catalyzes the synthesis of cardiolipin, a phospholipid component of mitochondrial membranes that is critical for mitochondrial function. [provided by RefSeq, Apr 2016],

CRNN抗體應(yīng)用：WB 1:500-2000 ELISA 1:5000-20000cornulin(CRNN) Homo sapiens This gene encodes a member of the "fused gene" family of proteins, which contain N-terminus EF-hand domains and multiple tandem peptide repeats. The encoded protein contains two EF-hand Ca2+ binding domains in its N-terminus and two glutamine- and threonine-rich 60 amino acid repeats in its C-terminus. This gene, also known as squamous epithelial heat shock protein 53, may play a role in the mucosal/epithelial immune response and epidermal differentiation. [provided by RefSeq, Jan 2009],