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ornithine aminotransferase Rabbit pAb (bs-18036R)  
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產(chǎn)品編號 bs-18036R
英文名稱 ornithine aminotransferase Rabbit pAb
中文名稱 鳥氨酸氨基轉移酶抗體
別    名 GACR; Gyrate atrophy; HOGA; OAT_HUMAN; Ornithine aminotransferase, hepatic form; Ornithine aminotransferase, renal form; OAT; OATASE; OKT; Ornithine aminotransferase(gyrate atrophy); Ornithine aminotransferase mitochondrial; ornithine aminotransferase pre  
研究領域 細胞生物  神經(jīng)生物學  信號轉導  細胞類型標志物  新陳代謝  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 Human,Mouse,Rat (predicted: Pig,Cow,Chicken,Horse)
產(chǎn)品應用 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
檢測分子量
細胞定位 細胞漿 線粒體
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ornithine aminotransferase: 351-439/439 
亞    型 IgG
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 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 OAT (ornithine aminotransferase (mitochondrial), ornithine-oxo-acid aminotransferase) is a 439 amino acid protein encoded by the human gene OAT. OAT belongs to the class III pyridoxal-phosphate-dependent aminotransferase family and is usually found as a homotetramer in the mitochondrion matrix. OAT catalyzes the major catalytic reaction for ornithine. Ornithinemia, presumably due to deficiency of ornithine ketoacid aminotransferase (OAT) has been found in patients with gyrate atrophy of the choroid and retina. The clinical history of gyrate atrophy is usually night blindness that begins in late childhood, accompanied by sharply demarcated circular areas of chorioretinal atrophy. During the second and third decades the areas of atrophy enlarge. The hepatic cleavage product, hepatic OAT, is formed by cleaving a 25 amino acid transit peptide from the N-terminus of the OAT precursor. The renal form is produced by cleaving a 35 amino acid transit peptide from the N-terminus。

Function:
Ornithine aminotransferase (OAT) is a key mitochondrial enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. OAT has also been linked with prostate cancer and alternatively activated macrophages

Subcellular Location:
Mitochondrion matrix.

SWISS:
P04181

Gene ID:
4942

Database links:

Entrez Gene: 4942 Human

Entrez Gene: 426430 Chicken

Entrez Gene: 505323 Cow

Entrez Gene: 18242 Mouse

Entrez Gene: 64313 Rat

Omim: 613349 Human

SwissProt: Q3ZCF5 Cow

SwissProt: P04181 Human

SwissProt: P29758 Mouse

SwissProt: P04182 Rat

Unigene: 523332 Human

Unigene: 13694 Mouse

Unigene: 1430 Rat



產(chǎn)品圖片
Sample: A431(Human) Cell Lysate at 30 ug Small intestine (Mouse) Lysate at 40 ug Primary: Anti- ornithine aminotransferase (bs-18036R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 45 kD Observed band size: 45 kD
Paraformaldehyde-fixed, paraffin embedded (rat 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 (ornithine aminotransferase) Polyclonal Antibody, Unconjugated (bs-18036R) at 1:200 overnight at 4°C, followed by operating according to SP Kit(Rabbit) (sp-0023) instructionsand DAB staining.
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