Product Name	CXorf36
Chinese Name	脱羧酶蛋白体36抗体
Alias	Deleted in autism 1 related protein; DIA1R; EPQL1862; hCG_1981635; hCG1981635; PRO3743; UPF0672 protein CXorf36; chromosome X open reading frame 36, isoform CRA_a; uncharacterized protein Cxorf36 precursor; PRO3743; EPQL1862; FLJ14103; FLJ55198; FLJ55198,; bA435K1.1; 4930578C19Rik; DKFZp313K0825; DIA1R_HUMAN; CXorf36.
Research Area	immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	Mouse,  (predicted: Human, )
Applications	WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=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	45kDa
Cellular localization	Extracellular matrix
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human CXorf36: 101-182/182
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 CXorf36 gene product has been provisionally designated CXorf36 pending further characterization. Subcellular Location: Secreted (Potential). DISEASE: Note=Genetic variations in CXorf36 may be associated with susceptibility to autism. Similarity: Belongs to the DIA1 family. SWISS: Q9H7Y0 Gene ID: 79742 Database links: Entrez Gene: 79742 Human SwissProt: Q9H7Y0 Human Unigene: 98321 Human
Product Picture	Sample: Cerebrum (Mouse) Lysate at 40 ug Primary: Anti-CXorf36 (SL0727R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 45 kD Observed band size: 50 kD Sample: Kidney(Mouse) lysate at 60ug; Liver(Mouse) lysate at 60ug; Primary: Anti-CXorf36 (SL0727R) at 1:300; Secondary: HRP conjugated Goat-Anti-Rabbit IgG(SL0295G-HRP) at 1: 5000; Predicted band size :45 kD Observed band size :50/75 kD Sample: Lung (Mouse) Lysate at 40 ug Primary: Anti-CXorf36 (SL0727R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 45 kD Observed band size: 50 kD Paraformaldehyde-fixed, paraffin embedded (Mouse brain); Antigen retrieval by boiling in sodium citrate buffer (pH6.0) for 15min; Block endogenous peroxidase by 3% hydrogen peroxide for 20 minutes; Blocking buffer (normal goat serum) at 37°C for 30min; Antibody incubation with (CXorf36) Polyclonal Antibody, Unconjugated (SL0727R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.

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