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CXorf36 Rabbit pAb (bs-0727R)  
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產(chǎn)品編號(hào) bs-0727R
英文名稱 CXorf36 Rabbit pAb
中文名稱 脫羧酶蛋白體36抗體
別    名 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.  
研究領(lǐng)域 免疫學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號(hào)
交叉反應(yīng) Mouse (predicted: Human)
產(chǎn)品應(yīng)用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 45 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞外基質(zhì) 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human CXorf36: 101-182/182 
亞    型
純化方法 affinity purified by Protein A
緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事項(xiàng) This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
產(chǎn)品介紹 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



產(chǎn)品圖片
Sample: Kidney(Mouse) lysate at 60ug; Liver(Mouse) lysate at 60ug; Primary: Anti-CXorf36 (bs-0727R) at 1:300; Secondary: HRP conjugated Goat-Anti-Rabbit IgG(bs-0295G-HRP) at 1: 5000; Predicted band size :45 kD Observed band size :50/75 kD
Sample: Lane 1: Mouse Cerebellum tissue lysates Lane 2: Mouse Cerebrum tissue lysates Primary: Anti-CXorf36 (bs-0727R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 45 kDa Observed band size: 46 kDa
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 (bs-0727R) at 1:400 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
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