C5ORF49 antibody (AA 1-100) (HRP)

Catalog No. ABIN1712492

The Rabbit Polyclonal anti-C5ORF49 antibody is suitable to detect C5ORF49 in samples from Human. It has been validated for WB, ELISA, IHC (fro) and IHC (p).

Quick Overview for C5ORF49 antibody (AA 1-100) (HRP) (ABIN1712492)

Target: C5ORF49 (Chromosome 5 Open Reading Frame 49 (C5ORF49))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C5ORF49 antibody is conjugated to HRP

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

Product Details anti-C5ORF49 Antibody (HRP)

Binding Specificity: AA 1-100

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C5orf49

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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.

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 C5ORF49

Target: C5ORF49 (Chromosome 5 Open Reading Frame 49 (C5ORF49))

Alternative Name: C5orf49

Background:

Synonyms: C5orf49, CE049_HUMAN, Chromosome 5 open reading frame 49, Uncharacterized protein C5orf49.

Background: C5orf49 is a With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome. The C5orf49 gene product has been provisionally designated C5orf49 pending further characterization.

Gene ID: 134121