RBM28 antibody (C-Term)

Catalog No. ABIN2856748

This Rabbit Polyclonal antibody specifically detects RBM28 in WB, ICC and IF. It exhibits reactivity toward Human.

Quick Overview for RBM28 antibody (C-Term) (ABIN2856748)

Target: RBM28 (RNA Binding Motif Protein 28 (RBM28))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RBM28 antibody is un-conjugated

Application: Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)

Product Details anti-RBM28 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human

Characteristics: Rabbit Polyclonal antibody to RBM28 (RNA binding motif protein 28)
RBM28 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human RBM28. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: 293T

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for RBM28

Target: RBM28 (RNA Binding Motif Protein 28 (RBM28))

Alternative Name: RNA binding motif protein 28

Background: The protein encoded by this gene is a specific nucleolar component of the spliceosomal small nuclear ribonucleoprotein (snRNP)complexes . It specifically associates with U1, U2, U4, U5, and U6 small nuclear RNAs (snRNAs), possibly coordinating their transition through the nucleolus. Mutation in this gene causes alopecia, progressive neurological defects, and endocrinopathy (ANE syndrome), a pleiotropic and clinically heterogeneous disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Cellular Localization: Nucleus , nucleolus

Molecular Weight: 86 kDa

Gene ID: 55131

UniProt: Q9NW13

Pathways: SARS-CoV-2 Protein Interactome