丁香五月亚洲激情,自拍另类图片区亚洲

您好，歡迎來到拜力生物網(wǎng)站！請登錄注冊

我的訂單 | 聯(lián)系我們 | 在線客服QQ：3012681483 | 客服電話：400-968-7988 | 工作時間：08:30-17:30

主營產(chǎn)品： ELISA試劑盒、抗體、補體血清、兔補體、干擾素、小鼠測溫儀、進口試劑、Quidel代理、Swant代理、PBL Assay Science代理

網(wǎng)站首頁產(chǎn)品中心代理品牌新聞資訊資源中心關(guān)于我們

所在位置：首頁 > 產(chǎn)品中心 > Antibodies > Antibodies產(chǎn)品

訂購信息

上海拜力生物科技公司

Tel:400-968-7988 021-33779008

Anti-SLC25A13 Antibody

品牌：Antibodies

貨號：

規(guī)格：100μl

貨期：

應(yīng)用：

咨詢客服

立即購買加入購物車

Anti-SLC25A13 Antibody

商品詳情參考文獻相關(guān)資料

Overview

Name:	Anti-SLC25A13 Antibody See all SLC25A13 primary antibodies
Description:	Rabbit polyclonal antibody to SLC25A13
Specificity:	The antibody detects endogenous levels of total SLC25A13 protein.
Applications:	WB, IHC
Reactivity:	Human
Immunogen:	Fusion protein of human SLC25A13
Host:	Rabbit
Clonality:	Polyclonal
Conjugate:	Unconjugated
Purification:	Antigen affinity purification.
Concentration:	1.1mg / ml
Formulation:	Rabbit IgG in pH7.4 PBS, 0.05% NaN3, 40% Glycerol.
Storage:	Store at -20?C

Target

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.
Tissue Specificity:	High levels in liver and low levels in kidney, pancreas, placenta, heart and brain.
Involvement in Disease:	Citrullinemia 2: A form of citrullinemia, an autosomal recessive disease characterized primarily by elevated serum and urine citrulline levels. Ammonia intoxication is another manifestation. Citrullinemia type 2 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. Cholestasis, neonatal intrahepatic, caused by citrin deficiency: A form of citrullinemia type 2 with neonatal onset, characterized by suppression of the bile flow, hepatic fibrosis, low birth weight, growth retardation, hypoproteinemia, variable liver dysfunction. Neonatal intrahepatic cholestasis due to citrin deficiency 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.
Sequence Similarities:	Belongs to the mitochondrial carrier (TC 2.A.29) family.
Cellular Location:	Mitochondrion inner membrane.
Database Links:	Entrez Gene: 10165?Human Omim: 603859?Human SwissProt: Q9UJS0?Human Unigene: 489190?Human
Synonyms:	AI785475 Antibody ARALAR2 Antibody Calcium binding mitochondrial carrier protein Aralar2 Antibody Calcium-binding mitochondrial carrier protein Aralar2 Antibody Citrin Antibody CMC2_HUMAN Antibody CTLN2 Antibody Ctrn Antibody Mitochondrial aspartate glutamate carrier 2 Antibody RGD1565889 Antibody SLC25A13 Antibody Solute carrier family 25 (citrin) member 13 Antibody Solute carrier family 25 member 13 Antibody Solute carrier family 25 member 13 (citrin) Antibody
Information:	Target information shown above is from the UniProt Consortium.