C5orf35 antibody (AA 1-100) (FITC)

Catalog No. ABIN1709340

This anti-C5orf35 antibody is a Rabbit Polyclonal antibody detecting C5orf35 in WB, IF (p) and IF (cc). Suitable for Human.

Quick Overview for C5orf35 antibody (AA 1-100) (FITC) (ABIN1709340)

Target: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C5orf35 antibody is conjugated to FITC

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

Product Details anti-C5orf35 Antibody (FITC)

Binding Specificity: AA 1-100

Predicted Reactivity: Human,Dog

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C5orf35

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 C5orf35

Target: C5orf35 (Chromosome 5 Open Reading Frame 35 (C5orf35))

Alternative Name: C5orf35

Background:

Synonyms: C5orf35 chromosome 5 open reading frame 35, Chromosome 5 open reading frame 35, Hypothetical protein LOC133383, MGC33648, Uncharacterized protein C5orf35, SET domain-containing protein 9, SETD9_HUMAN.

Background: C5orf35 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 C5orf35 gene product has been provisionally designated C5orf35 pending further characterization.

Gene ID: 133383