C7ORF26 antibody (AA 1-100) (HRP)

Catalog No. ABIN1711559

The Rabbit Polyclonal anti-C7ORF26 antibody is suitable to detect C7ORF26 in samples from Human. It has been validated for WB, IHC (fro) and IHC (p).

Quick Overview for C7ORF26 antibody (AA 1-100) (HRP) (ABIN1711559)

Target: C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7ORF26 antibody is conjugated to HRP

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

Product Details anti-C7ORF26 Antibody (HRP)

Binding Specificity: AA 1-100

Purpose: C7orf26 Polyclonal Antibody, HRP Conjugated

Predicted Reactivity: Human,Mouse,Rat,Dog,Cow,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf26

Isotype: IgG

Application Details

Application Notes: WB(1:300-5000),

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Handling Advice: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C7ORF26

Target: C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))

Alternative Name: C7orf26

Background:

Synonyms: Chromosome 7 open reading frame 26, MGC2718, Uncharacterized protein C7orf26,CG026_HUMAN.

Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf26 gene product has been provisionally designated C7orf26 pending further characterization.