Full Product Name
CNNM4 Antibody
Product Synonym Names
Metal transporter CNNM4; Ancient conserved domain-containing protein 4; Cyclin-M4; CNNM4; ACDP4 KIAA1592
Product Gene Name
anti-CNNM4 antibody
[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for Q6P4Q7
Purity/Purification
>95%
Protein G Purified
Immunogen
Recombinant Human Metal transporter CNNM4 protein (589-691AA)
Preservative
0.03% Proclin 300
Constituents
50% Glycerol, 0.01M PBS, pH 7.4
Preparation and Storage
Upon receipt, store at-20 degree C or-80 degree C. Avoid repeated freeze.
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of anti-CNNM4 antibody 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.
Product Categories/Family for anti-CNNM4 antibody
Neuroscience
Applications Tested/Suitable for anti-CNNM4 antibody
ELISA (EIA), Immunohistochemistry (IHC), Immunofluorescence (IF)
Application Notes for anti-CNNM4 antibody
IHC: 1:200-1:500
IF: 1:50-1:200
Immunohistochemistry (IHC) of anti-CNNM4 antibody
IHC image of CSB-PA764727LA01HU diluted at 1:300 and staining in paraffin-embedded human small intestine tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4 degree C overnight. The primary is detected by a biotinylated secondary antibody and visualized using an HRP conjugated SP system.

Immunofluorescence (IF) of anti-CNNM4 antibody
Immunofluorescence staining of Hela cells with CSB-PA764727LA01HU at 1:100, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeabilized using 0.2% Triton X-100 and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4 degree C. The secondary antibody was Alexa Fluor 488-congugated AffiniPure Goat Anti-Rabbit IgG(H+L).

NCBI/Uniprot data below describe general gene information for CNNM4. It may not necessarily be applicable to this product.
NCBI Accession #
NP_064569.3
[Other Products]
NCBI GenBank Nucleotide #
NM_020184.4
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UniProt Primary Accession #
Q6P4Q7
[Other Products]
UniProt Secondary Accession #
Q53RE5; Q9H9G3; Q9HCI0; Q9NRN1; B7Z1U0; C7SQM3; C7SQM4; C7SQM5[Other Products]
UniProt Related Accession #
Q6P4Q7[Other Products]
Molecular Weight
29,485 Da
NCBI Official Full Name
metal transporter CNNM4
NCBI Official Synonym Full Names
cyclin and CBS domain divalent metal cation transport mediator 4
NCBI Official Symbol
CNNM4 [Similar Products]
NCBI Official Synonym Symbols
ACDP4
[Similar Products]
NCBI Protein Information
metal transporter CNNM4
UniProt Protein Name
Metal transporter CNNM4
UniProt Synonym Protein Names
Ancient conserved domain-containing protein 4; Cyclin-M4
Protein Family
Metal transporter
UniProt Gene Name
CNNM4 [Similar Products]
UniProt Synonym Gene Names
ACDP4; KIAA1592 [Similar Products]
NCBI Summary for CNNM4
This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]
UniProt Comments for CNNM4
Probable metal transporter. The interaction with the metal ion chaperone COX11 suggests that it may play a role in sensory neuron functions (). May play a role in biomineralization and retinal function.
Research Articles on CNNM4
1. Jalili Syndrome is a rare cone-rod dystrophy (CORD) and amelogenesis imperfecta (AI), We have further characterized its ocular phenotype, including describing SD-OCT, FAF, and electrophysiological features; and report several novel disease-causing sequence variants.
Precautions
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Disclaimer
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