IFRD1 antibody

Catalog No. ABIN2855855

The Rabbit Polyclonal anti-IFRD1 antibody has been validated for WB, IF and ICC. It is suitable to detect IFRD1 in samples from Human.

Quick Overview for IFRD1 antibody (ABIN2855855)

Target: IFRD1 (Interferon Related Developmental Regulator 1 (IFRD1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This IFRD1 antibody is un-conjugated

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

Product Details anti-IFRD1 Antibody

Cross-Reactivity: Human

Characteristics: Rabbit Polyclonal antibody to IFRD1 (interferon-related developmental regulator 1)
IFRD1 antibody

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human IFRD1. 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: Molt-4 , Raji

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.62 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 IFRD1

Target: IFRD1 (Interferon Related Developmental Regulator 1 (IFRD1))

Alternative Name: interferon related developmental regulator 1

Background: This gene is an immediate early gene that encodes a protein related to interferon-gamma. This protein may function as a transcriptional co-activator/repressor that controls the growth and differentiation of specific cell types during embryonic development and tissue regeneration. Mutations in this gene are associated with sensory/motor neuropathy with ataxia. This gene may also be involved in modulating the pathogenesis of cystic fibrosis lung disease. Alternate splicing results in multiple transcript variants.

Molecular Weight: 50 kDa

Gene ID: 3475

UniProt: O00458