ARG47164

anti-MCFD2 antibody

anti-MCFD2 antibody for IHC-Formalin-fixed paraffin-embedded sections and Human

Overview

Product Description Mouse Monoclonal antibody recognizes MCFD2
Tested Reactivity Hu
Tested Application IHC-P
Host Mouse
Clonality Monoclonal
Isotype IgG2a
Target Name MCFD2
Antigen Species Human
Immunogen Recombinant protein of Human MCFD2.
Conjugation Un-conjugated
Alternate Names MCFD2; Multiple coagulation factor deficiency protein 2; SDNSF; Neural stem cell-derived neuronal survival protein

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purification with Protein A
Buffer PBS, 0.09% Sodium azide, 50% Glycerol and 0.5% BSA
Preservative 0.09% Sodium azide
Stabilizer 50% Glycerol and 0.5% BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 90411 Human MCFD2

Swiss-port # Q8NI22 Human Multiple coagulation factor deficiency protein 2

Gene Symbol MCFD2
Gene Full Name multiple coagulation factor deficiency 2, ER cargo receptor complex subunit
Background This gene encodes a soluble luminal protein with two calmodulin-like EF-hand motifs at its C-terminus. This protein forms a complex with LMAN1 (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. [provided by RefSeq, Apr 2016]
Function The MCFD2-LMAN1 complex forms a specific cargo receptor for the ER-to-Golgi transport of selected proteins. Plays a role in the secretion of coagulation factors. [UniProt]
Cellular Localization Golgi apparatus. [UniProt]
Calculated MW 16 kDa
PTM Phosphoprotein. [UniProt]