CNNM4 antibody (C-Term)

Catalog No. ABIN7468182

This Rabbit Polyclonal antibody specifically detects CNNM4 in WB and IHC (p). It exhibits reactivity toward Human.

Quick Overview for CNNM4 antibody (C-Term) (ABIN7468182)

Target: CNNM4 (Cyclin M4 (CNNM4))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CNNM4 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-CNNM4 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human Cyclin M4. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: U87-MG

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.84 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for CNNM4

Target: CNNM4 (Cyclin M4 (CNNM4))

Alternative Name: cyclin and CBS domain divalent metal cation transport mediator 4

Background:

Synonyms: cyclin and CBS domain divalent metal cation transport mediator 4 , ACDP4

Background: 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]

Molecular Weight: 87 kDa

Gene ID: 26504

UniProt: Q6P4Q7