WBSCR1 Antibody | 29-458

WBSCR1 Antibody | 29-458 | Gentaur UK, US & Europe Distribution

Host: Rabbit

Reactivity: Human, Dog

Homology: N/A

Immunogen: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human WBSCR1.

Research Area: Other

Tested Application: E, WB, IHC

Application: WBSCR1 antibody can be used for detection of WBSCR1 by ELISA at 1:312500. WBSCR1 antibody can be used for detection of WBSCR1 by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50, 000 - 100, 000.

Specificiy: N/A

Positive Control 1: Cat. No. 1205 - Jurkat Cell Lysate

Positive Control 2: N/A

Positive Control 3: N/A

Positive Control 4: N/A

Positive Control 5: N/A

Positive Control 6: N/A

Molecular Weight: 27 kDa, 27 kDa

Validation: N/A

Isoform: N/A

Purification: Antibody is purified by protein A chromatography method.

Clonality: Polyclonal

Clone: N/A

Isotype: N/A

Conjugate: Unconjugated

Physical State: Liquid

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.

Concentration: batch dependent

Storage Condition: For short periods of storage (days) store at 4˚C. For longer periods of storage, store WBSCR1 antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Alternate Name: WBSCR1, WSCR1, WBSCR1, eIF-4H

User Note: Optimal dilutions for each application to be determined by the researcher.

BACKGROUND: WBSCR1 is one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization.This gene encodes one of the translation initiation factors, which functions to stimulate the initiation of protein synthesis at the level of mRNA utilization. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternative splicing of this gene generates 2 transcript variants.