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Multiple Coagulation Factor Deficiency 2, Recombinant Protein

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产品名称: Multiple Coagulation Factor Deficiency 2, Recombinant Protein
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简单介绍

Multiple Coagulation Factor Deficiency 2, Recombinant Protein


Multiple Coagulation Factor Deficiency 2, Recombinant Protein  的详细介绍
Product Name

Multiple Coagulation Factor Deficiency 2 (MCFD2), Recombinant Protein

Full Product Name

Multiple Coagulation Factor Deficiency 2, Recombinant, Human (MCFD2, T7-tagged, SDNSF, LMAN1IP)

Product Gene Name

MCFD2 recombinant protein

[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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Sequence
MASMTGGQQM GRGSHMEEPA ASFSQPGSMG LDKNTVHDQE HIMEHLEGVI NKPEAEMSPQ ELQLHYFKMH DYDGNNLLDG LELSTAITHV HKEEGSEQAP LMSEDELINI IDGVLRDDDK NNDGYIDYAE FAKSLQ
Chromosome Location
Chromosome: 2; NC_000002.11 (47129009..47168994, complement). Location: 2p21
OMIM
607788
3D Structure
ModBase 3D Structure for Q8NI22
Host
E Coli
Purity/Purification
Affinity Purified
~90% by SDS-PAGE.
Form/Format
Supplied as a liquid in 20mM Tris-HCl buffer, pH7.5,100mM NaCl,10% glycerol.
Endotoxin Level
1EU/1ug (LAL).
Preparation and Storage
May be stored at 4 degree C for short-term only. Aliquot to avoid repeated freezing and thawing. Store at -20 degree C. Aliquots are stable for at least 6 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
Other Notes
Small volumes of MCFD2 recombinant protein vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
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Related Product Information for
MCFD2 recombinant protein
Multiple coagulation factor deficiency 2 (MCFD2), also known as SDNSF. This is expressed by neural stem/progenitor cells of the hippocampus, and localized to region where neurogenesis persists throughout life. It has been found to prevent NSC cell death and to maintain stem cell characteristics. This protein forms a complex with LAMN1 that facilitates the transport of coagulation factors V and VIII from the endoplasmic reticulum to the Golgi apparatus via an endoplasmic reticulum Golgi intermediate compartment. Mutations in the MCFD2 gene may cause Factor V and Factor VIII combined deficiency.

Recombinant human MCFD2, fused to T7-tag at N-terminus, was expressed in E.coli and purified by using conventional chromatography techniques.
Product Categories/Family for MCFD2 recombinant protein
Molecular Biology; MB-Coagulation Factors
Applications Tested/Suitable for MCFD2 recombinant protein
Western Blot (WB)
Application Notes for MCFD2 recombinant protein
Suitable for use in Western Blot.
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NCBI/Uniprot data below describe general gene information for MCFD2. It may not necessarily be applicable to this product.
NCBI GI #
284005451
NCBI GeneID
90411
NCBI Accession #
NP_001164977.1 [Other Products]
NCBI GenBank Nucleotide #
NM_001171506.2 [Other Products]
UniProt Primary Accession #
Q8NI22 [Other Products]
UniProt Secondary Accession #
Q53SS3; Q68D61; Q8N3M5; A8K7W2; D6W5A9; E9PD95[Other Products]
UniProt Related Accession #
Q8NI22[Other Products]
Molecular Weight
15.1kD[Similar Products]
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NCBI Official Full Name
multiple coagulation factor deficiency protein 2 isoform A
NCBI Official Synonym Full Names
multiple coagulation factor deficiency 2
NCBI Official Symbol
MCFD2  [Similar Products]
NCBI Official Synonym Symbols
F5F8D; SDNSF; F5F8D2; LMAN1IP
  [Similar Products]
NCBI Protein Information
multiple coagulation factor deficiency protein 2; neural stem cell derived neuronal survival protein; neural stem cell-derived neuronal survival protein
UniProt Protein Name
Multiple coagulation factor deficiency protein 2
UniProt Synonym Protein Names
Neural stem cell-derived neuronal survival protein
Protein Family
Multiple coagulation factor deficiency protein
UniProt Gene Name
MCFD2  [Similar Products]
UniProt Synonym Gene Names
SDNSF  [Similar Products]
UniProt Entry Name
MCFD2_HUMAN
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NCBI Summary for MCFD2
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 ***** 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, Jun 2010]
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UniProt Comments for MCFD2
MCFD2: 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. Defects in MCFD2 are a cause of factor V and factor VIII combined deficiency type 2 (F5F8D2); also known as multiple coagulation factor deficiency 2 (MCFD2). F5F8D2 is a blood coagulation disorder characterized by bleeding symptoms similar to those in hemophilia or parahemophilia, that are caused by single deficiency of FV or FVIII, respectively. The most common symptoms are epistaxis, menorrhagia, and excessive bleeding during or after trauma. Plasma levels of coagulation factors V and VIII are in the range of 5 to 30% of normal. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Endoplasmic reticulum

Chromosomal Location of Human Ortholog: 2p21

Cellular Component: Golgi apparatus; endoplasmic reticulum; ER-Golgi intermediate compartment

Molecular Function: calcium ion binding

Biological Process: vesicle-mediated transport; protein transport; cellular protein metabolic process; protein amino acid N-linked glycosylation via asparagine; post-translational protein modification

Disease: Factor V And Factor Viii, Combined Deficiency Of, 2
Research Articles on MCFD2
1. Data indicate that together with its soluble coreceptor MCFD2, LMAN1 transports coagulation factors V (FV) and VIII (FVIII).
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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