C7ORF25 antibody (AA 1-100) (AbBy Fluor® 555)

Catalog No. ABIN1697573

Product Details anti-C7ORF25 Antibody (AbBy Fluor® 555)

Target: C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))

Binding Specificity: AA 1-100

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7ORF25 antibody is conjugated to AbBy Fluor® 555

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf25

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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, 0.03 % 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.

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 C7ORF25

Target: C7ORF25 (Chromosome 7 Open Reading Frame 25 (C7ORF25))

Alternative Name: C7orf25 (C7ORF25 Products)

Synonyms: C7orf25 antibody, c7orf25 antibody, chromosome 7 open reading frame 25 antibody, chromosome 4 open reading frame, human C7orf25 antibody, expressed sequence AW209491 antibody, similar to expressed sequence AW209491 antibody, chromosome 7 open reading frame 25 L homeolog antibody, C7orf25 antibody, C4H7orf25 antibody, AW209491 antibody, RGD1308147 antibody, c7orf25.L antibody

Background:

Synonyms: C7orf25, CG025_HUMAN, Chromosome 7 open reading frame 25, RGD1308147, UPF0415 protein C7orf25.

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 C7orf25 gene product has been provisionally designated C7orf25 pending further characterization.