CNNM4 antibody (AA 565-593)

Catalog No. ABIN5534944

Product Details anti-CNNM4 Antibody

Target: CNNM4 (Cyclin M4 (CNNM4))

Binding Specificity: AA 565-593

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CNNM4 antibody is un-conjugated

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

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This CNNM4 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 565-593 amino acids from the Central region of human CNNM4.

Isotype: Ig Fraction

Application Details

Application Notes: For WB starting dilution is: 1:1000

For IHC-P starting dilution is: 1:50~100

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

Target Details for CNNM4

Target: CNNM4 (Cyclin M4 (CNNM4))

Alternative Name: CNNM4 (CNNM4 Products)

Synonyms: DKFZp468E0110 antibody, ACDP4 antibody, 5430430O18Rik antibody, Acdp4 antibody, cyclin and CBS domain divalent metal cation transport mediator 4 antibody, cyclin M4 antibody, CNNM4 antibody, CpipJ_CPIJ006743 antibody, cnnm4 antibody, Cnnm4 antibody

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