C7orf42 antibody (AA 231-314) (Alexa Fluor 555)

Catalog No. ABIN1697002

Product Details anti-C7orf42 Antibody (Alexa Fluor 555)

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Binding Specificity: AA 231-314

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C7orf42 antibody is conjugated to Alexa Fluor 555

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

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C7orf42

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 C7orf42

Target: C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))

Alternative Name: C7orf42 (C7orf42 Products)

Synonyms: C7orf42 antibody, c7orf42 antibody, TMEM248 antibody, MGC79534 antibody, C25H7orf42 antibody, 0610007L01Rik antibody, A930023A16Rik antibody, AW557951 antibody, G430067H08Rik antibody, zgc:103561 antibody, transmembrane protein 248 antibody, transmembrane protein 248 L homeolog antibody, TMEM248 antibody, tmem248.L antibody, tmem248 antibody, Tmem248 antibody

Background:

Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.

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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.

Gene ID: 55069