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The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. Additionally we are shipping RHD Kits (6) and and many more products for this protein.
Showing 10 out of 44 products:
Human Monoclonal RHD Primary Antibody for FACS, IP - ABIN260386
Avent, Judson, Parsons, Mallinson, Anstee, Tanner, Evans, Hodges, Maciver, Holmes et al.: Monoclonal antibodies that recognize different membrane proteins that are deficient in Rhnull human erythrocytes. One group of antibodies reacts with a variety of cells and tissues whereas the other ... in The Biochemical journal 1988
The RHD 1227G>A mutation contributes to the molecular basis of Del phenotype in the Taiwanese population. The point mutation results in aberrant frame shift or exon deletion transcripts and generates D protein with weak antigen presenting function.
In this mixed Brazilian population, the most frequent weak D types were 1, 4, 3 and 2 (frequencies of 4.35%, 2.32%, 1.46% and 0.29%, respectively; total of 8.41%) and partial D was found in 2.90% of samples carrying the RHD gene. For samples with inconclusive RhD typing, 53.33% of them presented weak and partial RHD, and 43.75% had concomitantly more than one RHD variant
Six weak D types in the Russian Federation: the most common type 3 (49.2%) and type 1 (28.6%), type 2 (14.3), type 15 (4.8%), type 4.2 (DAR) (1.6%) and type 6 (1.6%).
The frequency of RhD negative homozygosity in the Cypriot population was estimated to be 7.2%, while the frequencies of RHD hemizygosity and RhD positive homozygosity was calculated to be 39.2 and 53.6%, respectively.
Occurrence of partial RhD alleles in the Tunisian population.
The RHCE (show RHCE Antibodies) gene intron 4 of Han Chinese, Tibetans, and Mongols differs from the RHD gene intron 4 in the presence of a 652-bp fragment.
Reduced expression of D antigen is caused not only by missense mutation of the RHD gene, but also by silent mutation that may affect splicing.
Loss of heterozygosity of RhD gene on chromosome 1p in acute myeloid leukemia (show BCL11A Antibodies).
Rh antibodies in SCD (show SCD Antibodies) patients with RH variants can be clinically significant and, therefore, matching patients based on RH variants should be considered.
Paternal RHD zygosity determination in Tunisians: evaluation of three molecular tests.
The Rh blood group system is the second most clinically significant of the blood groups, second only to ABO. It is also the most polymorphic of the blood groups, with variations due to deletions, gene conversions, and missense mutations. The Rh blood group includes this gene, which encodes the RhD protein, and a second gene that encodes both the RhC and RhE antigens on a single polypeptide. The two genes, and a third unrelated gene, are found in a cluster on chromosome 1. The classification of Rh-positive and Rh-negative individuals is determined by the presence or absence of the highly immunogenic RhD protein on the surface of erythrocytes. Multiple transcript variants encoding different isoforms have been found for this gene.
D antigen (DCS)
, RH polypeptide 2
, Rh blood group antigen Evans
, Rh blood group, D anitgen
, Rhesus blood group D antigen allele DIII type 7
, Rhesus system D polypeptide
, blood group Rh(D) polypeptide
, rhesus D antigen
, Rh-like polypeptide
, Rhesus blood group CE and D
, erythrocyte membrane glycoprotein Rh30