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MCFD2 encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. Additionally we are shipping Multiple Coagulation Factor Deficiency 2 Antibodies (41) and Multiple Coagulation Factor Deficiency 2 Kits (5) and many more products for this protein.
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Human MCFD2 Protein expressed in Escherichia coli (E. coli) - ABIN666930
Mohanty, Ghosh, Shetty, Spreafico, Garagiola, Peyvandi: Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII. in American journal of hematology 2005
Show all 2 references for ABIN666930
Results indicate the biological roles of MCFD2 in both vertebrates and invertebrates.
A novel missense mutation, namely Asp81Ala in exon 3 of MCFD2 gene, is firstly reported and described as a cause of combined FV and FVIII (show F8 Proteins) deficiency in a Chinese family.
Studies indicate that the LMAN1 (show LMAN1 Proteins)-CRD (show CRX Proteins) contains distinct, separable binding sites for both its partner protein MCFD2 and the cargo proteins FV/FVIII (show F8 Proteins).
Data indicate that together with its soluble coreceptor MCFD2, LMAN1 (show LMAN1 Proteins) transports coagulation factors V (FV) and VIII (show COX8A Proteins) (FVIII (show F8 Proteins)).
Mutations in MCFD2 lead to F5F8D (show LMAN1 Proteins) (combined deficiency of factor V And factor VIII) due to alterations in MCFD2-LMAN1 (show LMAN1 Proteins) complex of coat protein (show GOLPH3 Proteins) (COP (show CARD16 Proteins))II complex trafficking machinery; 30% of F5F8D (show LMAN1 Proteins) patients have mutations in MCFD2. [REVIEW]
We present the identification of a novel MCFD2 gene missense mutation by direct sequencing.
The study reports for the first time a case of Combined factor V and factor VIII deficiency disorder in a Tunisian family, resulting from two novel mutations in exon 3 of the MCFD2 gene.
Data present the crystal structure of the LMAN1 (show LMAN1 Proteins)/MCFD2 complex and relate it to patient mutations. Circular dichroism data show that the majority of the substitution mutations give rise to a disordered or severely destabilized MCFD2 protein.
Data show that mutations in MCFD2 that disrupt the tertiary structure and abolish LMAN1 (show LMAN1 Proteins) binding still retain the FV/FVIII (show F8 Proteins) binding activities, suggesting that this interaction is independent of Ca(2 (show CA2 Proteins)+)-induced folding of the protein.
inactivating mutations in MCFD2 cause combined deficiency of factor V and factor VIII with a phenotype indistinguishable from that caused by mutations in LMAN1 (show LMAN1 Proteins)
This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LAMN1 (lectin mannose binding protein 1\; also known as ERGIC-53) that facilitates the transport of coagulation factors V (FV) and VIII (FVIII) from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment (ERGIC). Mutations in this gene cause combined deficiency of FV and FVIII (F5F8D)\; a rare autosomal recessive bleeding disorder characterized by mild to moderate bleeding and coordinate reduction in plasma FV and FVIII levels. This protein has also been shown to maintain stem cell potential in adult central nervous system and is a marker for testicular germ cell tumors. The 3' UTR of this gene contains a transposon-like human repeat element named 'THE 1'. A processed RNA pseudogene of this gene is on chromosome 6p22.1. Alternative splicing results in multiple transcript variants encoding distinct isoforms.
multiple coagulation factor deficiency 2
, multiple coagulation factor deficiency protein 2
, Multiple coagulation factor deficiency protein 2 homolog
, neural stem cell derived neuronal survival protein
, neural stem cell-derived neuronal survival protein
, multiple coagulation factor deficiency protein 2 homolog
, stem cell derived neuronal survival protein