RRBP1 antibody (C-Term)

Catalog No. ABIN7464588

This Mouse Monoclonal antibody specifically detects RRBP1 in WB, IF and ICC. It exhibits reactivity toward Human.

Quick Overview for RRBP1 antibody (C-Term) (ABIN7464588)

Target: RRBP1 (Ribosome Binding Protein 1 (RRBP1))

Reactivity: Human

Host: Mouse

Clonality: Monoclonal

Conjugate: This RRBP1 antibody is un-conjugated

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

Grade: KO Validated

Clone: GT5610

Product Details anti-RRBP1 Antibody

Binding Specificity: C-Term

Cross-Reactivity: Human

Purification: Affinity purified by Protein G.

Immunogen: Recombinant protein encompassing a sequence within the C-terminus region of human Ribosome binding protein 1. The exact sequence is proprietary.

Isotype: IgG2a

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:2000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: HepG2

Validation: KO/KD

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS, No Preservative

Preservative: Without preservative

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 RRBP1

Target: RRBP1 (Ribosome Binding Protein 1 (RRBP1))

Alternative Name: ribosome binding protein 1

Background: Ribosome binding protein 1 , ES/130 , ES130 , RRp , hES,Analysis of cDNA clones indicates that ribosome binding protein 1 may exist in different forms due to removal of tandem repeats, or partial intraexonic splicing of RRBP1. The form presented here is lacking the canine p180 ribosome-binding domain, NQGKKAEGAQ, which is tandemly repeated close to the N-terminus in other forms that haven't been fully characterized. RRBP1 has been excluded as a candidate gene in the cause of Alagille syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq]

Molecular Weight: 152 kDa

Gene ID: 6238

UniProt: Q9P2E9