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RabbitAnti-SLC25A38 Rabbit pAb  antibody (bs-19815R)
~~~促销,代码KXJ230206~~~
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说明书: 50ul  100ul  200ul
50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-19815R
英文名称 SLC25A38 Rabbit pAb
中文名称 溶质载体家族蛋白25成员38抗体
别    名 SIDBA2; appoptosin; RGD1311914; S2538_BOVIN; SLC25A38; Solute carrier family 25 member 38; S2538_HUMAN; Mitochondrial glycine transporter GlyC; S2538_MOUSE; S2538_RAT;   
研究领域 肿瘤  细胞生物  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 Mouse, Rat,  (predicted: Human, Cow, Rabbit, Sheep, )
产品应用 WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 (石蜡切片需做抗原修复)
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 34 kDa
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SLC25A38: 101-200/304 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia.[provided by RefSeq, Mar 2010]

Function:
Mitochondrial carrier required during erythropoiesis. Probably involved in the biosynthesis of heme, possibly by facilitating 5-aminolevulinate (ALA) production. May act by importing glycine into mitochondria or by exchanging glycine for ALA across the mitochondrial inner membrane.

Subcellular Location:
Mitochondrion inner membrane.

Tissue Specificity:
Preferentially expressed in erythroid cells.

DISEASE:
Defects in SLC25A38 are a cause of anemia sideroblastic pyridoxine-refractory autosomal recessive (PRARSA) [MIM:205950]. A form of sideroblastic anemia not responsive to pyridoxine. Sideroblastic anemia is characterized by anemia of varying severity, hypochromic peripheral erythrocytes, systemic iron overload secondary to chronic ineffective erythropoiesis, and the presence of bone marrow ringed sideroblasts. Sideroblasts are characterized by iron-loaded mitochondria clustered around the nucleus.

Similarity:
Belongs to the mitochondrial carrier family.
SLC25A38 subfamily.
Contains 3 Solcar repeats.

SWISS:
Q96DW6

Gene ID:
54977

Database links:

Entrez Gene: 512325 Cow

Entrez Gene: 54977 Human

Entrez Gene: 208638 Mouse

Entrez Gene: 301067 Rat

Entrez Gene: 100147784 Sheep

Omim: 610819 Human

SwissProt: Q5EAC0 Cow

SwissProt: Q96DW6 Human

SwissProt: Q91XD8 Mouse

SwissProt: Q499U1 Rat

SwissProt: S2538 Sheep

Unigene: 369615 Human

Unigene: 236656 Mouse

Unigene: 21048 Rat



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