Product Name
CDGSH iron-sulfur domain-containing protein 2 (CISD2), Recombinant Protein
Full Product Name
Recombinant Human CDGSH iron-sulfur domain-containing protein 2 (CISD2), partial
Product Gene Name
CISD2 recombinant protein
[Similar Products]
Product Synonym Gene Name
CISD2[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Sequence Positions
61-135
Sequence
PKKKQQKDSL INLKIQKENP KVVNEINIED LCLTKAAYCR CWRSKTFPAC DGSHNKHNEL TGDNVGPLIL KKKEV
3D Structure
ModBase 3D Structure for Q8N5K1
Host
E Coli or Yeast or Baculovirus or Mammalian Cell
Purity/Purification
>85% (SDS-PAGE) (lot specific)
Form/Format
Liquid containing glycerol
Tag Information
This protein contains an N-terminal tag and may also contain a C-terminal tag. Tag types are determined by various factors including tag-protein stability, please inquire for tag information.
Sterility
Sterile filter available upon request.
Endotoxin
Low endotoxin available upon request.
Storage Buffer
Tris-based buffer, 50% glycerol
Preparation and Storage
Store at -20 degrees C. For long-term storage, store at -20 degrees C or -80 degrees C. Store working aliquots at 4 degrees C for up to one week. Repeated freezing and thawing is not recommended.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of CISD2 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.
Related Product Information for
CISD2 recombinant protein
This protein is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron
sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2 (WFS2).
NCBI/Uniprot data below describe general gene information for CISD2. It may not necessarily be applicable to this product.
NCBI Accession #
NP_001008389.1
[Other Products]
NCBI GenBank Nucleotide #
NM_001008388.4
[Other Products]
UniProt Primary Accession #
Q8N5K1
[Other Products]
UniProt Secondary Accession #
Q7Z3D5[Other Products]
UniProt Related Accession #
Q8N5K1[Other Products]
Molecular Weight
15,278 Da
NCBI Official Full Name
CDGSH iron-sulfur domain-containing protein 2
NCBI Official Synonym Full Names
CDGSH iron sulfur domain 2
NCBI Official Symbol
CISD2 [Similar Products]
NCBI Official Synonym Symbols
ERIS; WFS2; ZCD2; NAF-1; Miner1
[Similar Products]
NCBI Protein Information
CDGSH iron-sulfur domain-containing protein 2
UniProt Protein Name
CDGSH iron-sulfur domain-containing protein 2
UniProt Synonym Protein Names
Endoplasmic reticulum intermembrane small protein; MitoNEET-related 1 protein; Miner1; Nutrient-deprivation autophagy factor-1; NAF-1
Protein Family
CDGSH iron-sulfur domain-containing protein
UniProt Gene Name
CISD2 [Similar Products]
UniProt Synonym Gene Names
CDGSH2; ERIS; ZCD2; Miner1; NAF-1 [Similar Products]
NCBI Summary for CISD2
The protein encoded by this gene is a zinc finger protein that localizes to the endoplasmic reticulum. The encoded protein binds an iron/sulfur cluster and may be involved in calcium homeostasis. Defects in this gene are a cause of Wolfram syndrome 2. [provided by RefSeq, Mar 2011]
UniProt Comments for CISD2
Regulator of autophagy that contributes to antagonize BECN1-mediated cellular autophagy at the endoplasmic reticulum. Participates in the interaction of BCL2 with BECN1 and is required for BCL2-mediated depression of endoplasmic reticulum Ca2+ stores during autophagy. Contributes to BIK-initiated autophagy, while it is not involved in BIK-dependent activation of caspases. Involved in life span control, probably via its function as regulator of autophagy.
Research Articles on CISD2
1. A mutation resulted in the loss of functional CISD2 protein in the two Italian Wolfram syndrome type 2 patients.">The c.103 + 1G > A mutation resulted in the loss of functional CISD2 protein in the two Italian Wolfram syndrome type 2 patients.
Precautions
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Disclaimer
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