RGF1C抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Guanine nucleotide exchange factor (GEF).,similarity:Contains 1 N-terminal Ras-GEF domain.,similarity:Contains 1 Ras-GEF domain.,

RGL1抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Probable guanine nucleotide exchange factor.,similarity:Contains 1 N-terminal Ras-GEF domain.,similarity:Contains 1 Ras-associating domain.,similarity:Contains 1 Ras-GEF domain.,subunit:Interacts with Ras.,tissue specificity:Expressed in a wide variety of tissues with strong expression being seen in the heart, brain, kidney, spleen and testis.,

RGL2抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:Probable guanine nucleotide exchange factor. Putative effector of Ras and/or Rap. Associates with the GTP-bound form of Rap 1A and H-Ras in vitro.,similarity:Contains 1 N-terminal Ras-GEF domain.,similarity:Contains 1 Ras-associating domain.,similarity:Contains 1 Ras-GEF domain.,

RGL3抗体应用：WB 1:500-2000

RGMA抗体应用：WB 1:500-2000 ELISA 1:5000-20000repulsive guidance molecule family member a(RGMA) Homo sapiens This gene encodes a member of the repulsive guidance molecule family. The encoded protein is a glycosylphosphatidylinositol-anchored glycoprotein that functions as an axon guidance protein in the developing and adult central nervous system. This protein may also function as a tumor suppressor in some cancers. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009],

RGMB抗体应用：WB 1:500-2000 ELISA 1:5000-20000repulsive guidance molecule family member b(RGMB) Homo sapiens RGMB is a glycosylphosphatidylinositol (GPI)-anchored member of the repulsive guidance molecule family (see RGMA, MIM 607362) and contributes to the patterning of the developing nervous system (Samad et al., 2005 [PubMed 15671031]).[supplied by OMIM, Apr 2009],

RGMC抗体应用：WB 1:500-2000 ELISA 1:5000-20000hemochromatosis type 2 (juvenile)(HFE2) Homo sapiens The product of this gene is involved in iron metabolism. It may be a component of the signaling pathway which activates hepcidin or it may act as a modulator of hepcidin expression. It could also represent the cellular receptor for hepcidin. Two uORFs in the 5' UTR negatively regulate the expression and activity of the encoded protein. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene. Defects in this gene are the cause of hemochromatosis type 2A, also called juvenile hemochromatosis (JH). JH is an early-onset autosomal recessive disorder due to severe iron overload resulting in hypogonadotrophic hypogonadism, hepatic fibrosis or cirrhosis and cardiomyopathy, occurring typically before age of 30. [provided by RefSeq, Oct 2015],

RGP1抗体应用：WB 1:500-2000

RGPA1抗体应用：WB 1:500-2000 ELISA 1:5000-20000Ral GTPase activating protein catalytic alpha subunit 1(RALGAPA1) Homo sapiens This gene encodes a major subunit of the RAL-GTPase activating protein. A similar protein in mouse binds E12, a transcriptional regulator of immunoglobulin genes. The mouse protein also functions in skeletal muscle by binding to the regulatory 14-3-3 proteins upon stimulation with insulin or muscle contraction. A pseudogene of this gene has been identified on chromosome 9. [provided by RefSeq, Oct 2016],

RGPD5抗体应用：WB 1:500-2000 ELISA 1:5000-20000RANBP2-like and GRIP domain containing 5(RGPD5) Homo sapiens RAN is a small GTP-binding protein of the RAS superfamily that is associated with the nuclear membrane and is thought to control a variety of cellular functions through its interactions with other proteins. This gene shares a high degree of sequence identity with RANBP2, a large RAN-binding protein localized at the cytoplasmic side of the nuclear pore complex. It is believed that this RANBP2 gene family member arose from a duplication event 3 Mb distal to RANBP2. Alternative splicing has been observed for this locus and two variants are described. Additional splicing is suggested but complete sequence for further transcripts has not been determined. [provided by RefSeq, Jul 2008],