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Rabbit Anti-BEND2 antibody
Rabbit Anti-BEND2 antibody
BEN domain-containing protein 2; BEN domain containing 2; BEND 2; BEND2; BEND-2; Chromosome X open reading frame 20; MGC33653; BEND2_HUMAN; CXorf56.
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Details

Product Name BEND2
Chinese Name BEND2蛋白抗体
Alias BEN domain-containing protein 2; BEN domain containing 2; BEND 2; BEND2; BEND-2; Chromosome X open reading frame 20; MGC33653; BEND2_HUMAN; CXorf56.  
Research Area Cell biology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species (predicted: Human, )
Applications WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (Paraffin sections need antigen repair)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight 88kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human BEND2/CXorf56: 101-200/799 
Lsotype IgG
Purification affinity purified by Protein A
Buffer Solution 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
Product Detail BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Similarity:
Contains 2 BEN domains.

SWISS:
Q8NDZ0

Gene ID:
139105

Database links:

Entrez Gene: 139105 Human

SwissProt: Q8NDZ0 Human



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