MCFD2 Monoclonal Antibody (294301) | Invitrogen MA5-24000 product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Invitrogen

other brands :

NeoMarkers, Lab Vision, Endogen, Pierce, BioSource International, Zymed Laboratories, Caltag, Molecular Probes, Research Genetics, Life Technologies, Applied Biosystems, GIBCO BRL, ABgene, Dynal, Affinity BioReagents, Nunc, Invitrogen, NatuTec, Oxoid, Richard-Allan Scientific, Arcturus, Perseptive Biosystems, Proxeon, eBioscience

product type :

antibody

product name :

MCFD2 Monoclonal Antibody (294301)

catalog :

MA5-24000

quantity :

100 ug

price :

US 414.00

clonality :

monoclonal

host :

mouse

conjugate :

nonconjugated

clone name :

294301

The same clone is also sold as:

R&D Systems: MAB2357

reactivity :

human

application :

western blot, immunohistochemistry

citations: 1

Reference
Stenson P, Mort M, Ball E, Evans K, Hayden M, Heywood S, et al. The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies. Hum Genet. 2017;136:665-677 pubmed publisher

product information

Product Type :

Antibody

Product Name :

MCFD2 Monoclonal Antibody (294301)

Catalog # :

MA5-24000

Quantity :

100 ug

Price :

US 414.00

Clonality :

Monoclonal

Purity :

Protein A/G

Host :

Mouse

Reactivity :

Human

Applications :

Immunohistochemistry: 8-25 ug/mL, Western Blot: 1 ug/mL

Species :

Human

Clone :

294301

Isotype :

IgG2b

Storage :

-20 C, Avoid Freeze/Thaw Cycles

Description :

Multiple coagulation factor deficiency protein 2 (MCFD2) is localized in the endoplasmic reticulum-Golgi intermediate compartment (ERGIC) through a direct, calcium-dependent interaction with LMAN1. The MCFD2-LMAN1 complex forms a specific cargo receptor for the transport of selected proteins from the endoplasmic reticulum to the Golgi apparatus. Mutations in the MCFD2 gene may cause of factor V and factor VIII combined deficiency (F5F8D). F5F8D is an autosomal recessive human bleeding disorder characterized by the reduction of both clotting proteins.

Immunogen :

E. coli-derived recombinant human SDNSF/MCFD2 Glu27-Gln146

Format :

Lyophilized

Applications w/Dilutions :

Immunohistochemistry: 8-25 ug/mL, Western Blot: 1 ug/mL

Aliases :

1810021C21Rik; F5F8D; F5F8D2; LMAN1IP; MCFD2; 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; Sdnsf; stem cell derived neuronal survival protein