SAMD14 antibody (PE-Cy5)

Catalog No. ABIN718358

The Rabbit Polyclonal anti-SAMD14 antibody is suitable to detect SAMD14 in samples from Human, Mouse, Rat, Cow and Dog. It has been validated for WB.

Quick Overview for SAMD14 antibody (PE-Cy5) (ABIN718358)

Target: SAMD14 (Sterile alpha Motif Domain Containing 14 (SAMD14))

Reactivity: Human, Mouse, Rat, Cow, Dog

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SAMD14 antibody is conjugated to PE-Cy5

Application: Western Blotting (WB)

Product Details anti-SAMD14 Antibody (PE-Cy5)

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human SAMD14

Isotype: IgG

Application Details

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.

Expiry Date: 12 months

Target Details for SAMD14

Target: SAMD14 (Sterile alpha Motif Domain Containing 14 (SAMD14))

Alternative Name: SAMD14

Background:

Synonyms: Sterile alpha motif domain-containing protein 14, SAM domain-containing protein 14, SAMD14

Background: The sterile alpha motif (SAM) domain is a 70 residue structure found in a large number of proteins involved in diverse processes present throughout eukaryotes. The SAM domain is known to bind RNA and is arranged in a small five-helix bundle with two large interfaces. SAMD14 (sterile alpha motif domain-containing protein 14) is a 417 amino acid protein encoded by the SAMD14 gene which maps to human chromosome 17. Chromosome 17 makes up over 2.5 % of the human genome with about 81 million bases encoding over 1,200 genes. Two key tumor suppressor genes are associated with chromosome 17, namely, p53 and BRCA1. Chromosome 17 is also linked to neurofibromatosis, a condition characterized by neural and epidermal lesions, and dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease.

Molecular Weight: 45kDa

Gene ID: 201191

UniProt: Q8IZD0