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BUD31 Polyclonal Antibody

BUD31 Polyclonal Antibody

Views(3) Publications(0) Catalog no(ABP50803)
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Specification

Product name BUD31 Polyclonal Antibody
Immunogen Synthesized peptide derived from the N-terminal region of human BUD31 at AA range: 10-90
Host Rabbit
Reactivity Human,Mouse,Rat
Applications WB,IHC,IF,ELISA
Applications notes Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:20000;IF 1:50-200
Clonality Polyclonal
Preparation method The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Alternative BUD31; EDG2; Protein BUD31 homolog; Protein EDG-2; Protein G10 homolog

Product Properties

Formulation Liquid solution
Concentration 1 mg/ml
Molecular weight 17kD
Storage buffer Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage instructions Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
Shipping Gel pack with blue ice.
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background BUD31 (Protein G10 homolog, EDG-2) is a 144 amino acid protein encoded by the human gene BUD31. BUD31 is a nuclear protein that belongs to the BUD31 (G10) family. BUD31 is found on chromosome 7 which is about 158 milllion bases long, encodes over 1,000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to osteogenesis imperfecta, Pendred syndrome, lissencephaly, citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the long (q) arm of human chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.
Gene ID 8896
Alternative BUD31; EDG2; Protein BUD31 homolog; Protein EDG-2; Protein G10 homolog
Others BUD31 Polyclonal Antibody detects endogenous levels of BUD31 protein.
Accession P41223
Observed Band(KD) 17

Image & description

Fig. Western Blot analysis of various cells using BUD31 Polyclonal Antibody.

Fig. Western Blot analysis of various cells using BUD31 Polyclonal Antibody.

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