DPY19L4 antibody (AA 75-180) (Biotin)

Catalog No. ABIN1398247

Product Details anti-DPY19L4 Antibody (Biotin)

Target: DPY19L4 (Dpy-19-Like 4 (DPY19L4))

Binding Specificity: AA 75-180

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This DPY19L4 antibody is conjugated to Biotin

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

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human DPY19L4

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.

Storage: -20 °C

Storage Comment: Store at -20°C for 12 months.

Expiry Date: 12 months

Target Details for DPY19L4

Target: DPY19L4 (Dpy-19-Like 4 (DPY19L4))

Alternative Name: DPY19L4 (DPY19L4 Products)

Synonyms: Gm1023 antibody, Narg3 antibody, RGD1305828 antibody, dpy-19 like 4 antibody, dpy-19-like 4 (C. elegans) antibody, DPY19L4 antibody, Dpy19l4 antibody

Background:

Synonyms: D19L4_HUMAN, Dpy 19 like 4, Dpy 19 like protein 4, Dpy-19-like protein 4, DPY19L4, MGC131885, Protein dpy 19 homolog 4, Protein dpy-19 homolog 4.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

Gene ID: 286148