C11orf46 antibody (PE)

Catalog No. ABIN2170734

This anti-C11orf46 antibody is a Rabbit Polyclonal antibody detecting C11orf46 in WB. Suitable for Human, Mouse and Rat.

Quick Overview for C11orf46 antibody (PE) (ABIN2170734)

Target: C11orf46 (Chromosome 11 Open Reading Frame 46 (C11orf46))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C11orf46 antibody is conjugated to PE

Application: Western Blotting (WB)

Product Details anti-C11orf46 Antibody (PE)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C11ORF46

Isotype: IgG

Application Details

Application Notes: FCM: (1:20-100)
Optimal working dilution should be determined by the investigator.

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: Sodium azide

Precaution of Use: This product contains Sodium azide: 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.

Target Details for C11orf46

Target: C11orf46 (Chromosome 11 Open Reading Frame 46 (C11orf46))

Alternative Name: C11ORF46

Background:

Synonyms: Chromosome 11 open reading frame 46, DJ299F11.1, FLJ38968, Hypothetical protein LOC120534, Uncharacterized protein C11orf46, AL14E_HUMAN.

Background: C11orf46, also known as FLJ38968 or dJ299F11.1, is a 260 amino acid protein that is encoded by a gene located on human chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 makes up around 4 % of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and _ thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

Gene ID: 120534