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Rabbit Anti-SLC25A13/Gold Conjugated antibody (bs-4038R-Gold)
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說 明 書: 100ul(10nm  15nm  35nm
100ul/2980.00元
大包裝/詢價
產品編號 bs-4038R-Gold
英文名稱 Rabbit Anti-SLC25A13/Gold Conjugated antibody
中文名稱 膠體金標記的線粒體內鈣結合天冬氨酸/谷氨酸載體蛋白抗體
別    名 ARALAR2; Calcium binding mitochondrial carrier protein Aralar2; Citrin; CTLN2; Ctrn; Mitochondrial aspartate glutamate carrier 2; RGD1565889; Solute carrier family 25 (citrin) member 13; Solute carrier family 25 member 13 (citrin); Solute carrier family 25 member 13; AI785475; CMC2_HUMAN.  
規格價格 100ul/2980元 購買        大包裝/詢價
說 明 書 100ul(10nm  15nm  35nm
研究領域 腫瘤  細胞生物  免疫學  神經生物學  結合蛋白  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human, Mouse, Rat, Chicken, Dog, Pig, Cow, Horse, )
產品應用 IEM=1:20-200 ICA=1:20-200 ChIP=1:20-200 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分 子 量 74kDa
性    狀 Lyophilized or Liquid
濃    度 0.4mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC25A13
亞    型 IgG
純化方法 affinity purified by Protein A
儲 存 液 0.02M TBS(pH8.2) with 1% BSA, 0.03% Proclin300.
保存條件 Store at 2-8 oC for 3-6 months. Avoid repeated freeze/thaw cycles.
產品介紹 background:
SLC25A13 is a member of the mitochondrial carrier family. It contains four EF-hand Ca(2+) binding motifs in the N-terminal domain, and localizes to mitochondria. It catalyzes the exchange of aspartate for glutamate and a proton across the inner mitochondrial membrane, and is stimulated by calcium on the external side of the inner mitochondrial membrane. Mutations in the SLC25A13 gene result in citrullinemia, type II. Multiple transcript variants encoding different isoforms have been found for this gene.

Function:
Catalyzes the calcium-dependent exchange of cytoplasmic glutamate with mitochondrial aspartate across the mitochondrial inner membrane. May have a function in the urea cycle.

Subcellular Location:
Mitochondrion inner membrane; Multi-pass membrane protein.

Tissue Specificity:
High levels in liver and low levels in kidney, pancreas, placenta, heart and brain.

DISEASE:
Defects in SLC25A13 are the cause of citrullinemia type 2 (CTLN2) [MIM:603471]. Citrullinemia belongs to the urea cycle disorders. It is an autosomal recessive disease characterized primarily by elevated serum and urine citrulline levels. Ammonia intoxication is another manifestation. CTLN2 is characterized by neuropsychiatric symptoms including abnormal behaviors, loss of memory, seizures and coma. Death can result from brain edema. Onset is sudden and usually between the ages of 20 and 50 years.
Defects in SLC25A13 are the cause of neonatal intrahepatic cholestasis due to citrin deficiency (NICCD) [MIM:605814]. NICCD is a form of citrullinemia type 2 with neonatal onset. NICCD is characterized by suppression of the bile flow, hepatic fibrosis, low birth weight, growth retardation, hypoproteinemia, variable liver dysfunction. NICCD is generally not severe and symptoms disappear by one year of age with an appropriate diet. Years or even decades later, however, some individuals develop the characteristic features of citrullinemia type 2 with neuropsychiatric symptoms.

Similarity:
Belongs to the mitochondrial carrier family.
Contains 4 EF-hand domains.
Contains 3 Solcar repeats.

Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

Citrin是一種線粒體內鈣結合天冬氨酸/谷氨酸載體(Aspartate/ Glutamate Carrier, AGC)蛋白,在尿素循環及其他代謝過程中發揮重要作用。Citrin缺乏癥包含成年發作Ⅱ型    瓜氨酸血癥(Adult Onset Type Ⅱ Citrullinemia , CTLN2)和Citrin缺乏所致新生兒肝內膽汁淤積癥( Neonatal Intrahepatic Cholestasis caused by Citrin Deficiency, NICCD)兩種不同表型,為常染色體隱性遺傳。
    Citrin分子量約為74kDa,含675個氨基酸,在肝臟、腎臟及心臟中均有表達,位于線粒體內膜。Citrin的N端有4個EF手型結構域,可結合鈣離子,C端作為線粒體載體活性部位有6個跨膜結構。研究還發現,Citrin的類似物-Aralar,同為天冬氨酸/谷氨酸載體蛋白,雖氨基酸序列與Citrin有77.8%的同源性,但組織分布明顯不同,Citrin主要在肝臟而Aralar 主要在骨骼肌和腦中表達,提示Citrin缺乏癥是一種局限于肝臟的疾病。
       Citrin作為肝內主要的天冬氨酸/谷氨酸載體蛋白,其功能有3方面;
其一,將線粒體中天冬氨酸轉運至胞漿中,參與尿素、蛋白和核酸的合成。
其二,將天冬氨酸轉運至胞漿,作為蘋果酸/天冬氨酸穿梭的一個環節,將胞漿中糖酵解生成的NADH還原當量運至線粒體內,參與能量、氨基酸、糖和脂代謝。
其三,在NADH形成及利用的同時促進乳糖糖異生。
     CTLN2患者多死于腦水腫,腦損傷機制尚不明確,高血氨并非唯一致病因素,局部缺血、能量耗竭、神經毒性及代謝失調引起氧化應激反應,均可加速腦損傷。CTLN2患者多并發肝臟腫瘤,其中大部分為肝細胞癌 。體外研究提示瓜氨酸的積聚對肝細胞的增生有促進作用,游離脂肪酸聚集造成的氧化應激和脂質過氧化反應對腫瘤發生也有重要作用。
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