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Rabbit Anti-CXorf56 antibody
Rabbit Anti-CXorf56 antibody
UPF0428 protein CXorf56; CX056_HUMAN.
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  • NO.:SL9550R
    Clonality:Polyclonal
    Immunogen Species:Rabbit
    React Species:Human,(predicted: Mouse,Rat,Chicken,Cow,Rabbit,Sheep,)
    Applications:WB ELISA IHC-P IHC-F ICC IF
    concentration:1mg/ml
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Details

Product Name CXorf56
Chinese Name X染色体开放阅读框56抗体
Alias UPF0428 protein CXorf56; CX056_HUMAN.  
Research Area Cell biology  immunology  Developmental biology  
Immunogen Species Rabbit
Clonality Polyclonal
React Species Human,  (predicted: Mouse, Rat, Chicken, Cow, Rabbit, Sheep, )
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 26kDa
Form Liquid
Concentration 1mg/ml
immunogen KLH conjugated synthetic peptide derived from human CXorf56: 121-222/222 
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 The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. 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. The CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.

Similarity:
Belongs to the UPF0428 family.

SWISS:
Q9H5V9

Gene ID:
63932

Database links:

Entrez Gene: 63932 Human

SwissProt: Q3T197 Cow

SwissProt: Q9H5V9 Human

SwissProt: Q8VDP2 Mouse

SwissProt: Q5U515 Xenopus laevis

SwissProt: Q66I61 Zebrafish

Unigene: 248572 Human



Product Picture
Sample: Raji Cell (Human) Lysate at 40 ug
Primary: Anti-CXorf56 (bs9550R) at 1/300 dilution
Secondary: HRP conjugated Goat-Anti-rabbit IgG (SL0295G-HRP) at 1/5000 dilution
Predicted band size: 26 kD
Observed band size: 26 kD

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