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Rabbit Anti-Glutaredoxin 5  antibody (bs-13395R)  
~~~促銷代碼KT202411~~~
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產品編號 bs-13395R
英文名稱 Rabbit Anti-Glutaredoxin 5  antibody
中文名稱 谷氧還蛋白5抗體
別    名 C14orf87; Chromosome 14 open reading frame 87; FLB4739; GLRX 5; Glrx5; GLRX5_HUMAN; Glutaredoxin 5 homolog; Glutaredoxin related protein 5; Glutaredoxin-related protein 5; Glutaredoxin5; GRX5; MGC14129; mitochondrial; Monothiol glutaredoxin-5; PRO1238.  
Specific References  (2)     |     bs-13395R has been referenced in 2 publications.
[IF=8.579] Lee J et al. Inhibition of Glutaredoxin 5 predisposes Cisplatin-resistant Head and Neck Cancer Cells to Ferroptosis. Theranostics. 2020 Jun 19;10(17):7775-7786.  WB ;  Human.  
[IF=5.008] Rychtarcikova, Zuzana, et al. "Tumor-initiating cells of breast and prostate origin show alterations in the expression of genes related to iron metabolism." Oncotarget (2016).  WB ;  Human.  
研究領域 腫瘤  細胞生物  信號轉導  新陳代謝  線粒體  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Pig,Sheep,Cow,Horse)
產品應用 WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 14kDa
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 Glutaredoxin 5: 51-157/157 
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
產品介紹 This gene encodes a mitochondrial protein, which is evolutionarily conserved. It is involved in the biogenesis of iron-sulfur clusters, which are required for normal iron homeostasis. Mutations in this gene are associated with autosomal recessive pyridoxine-refractory sideroblastic anemia. [provided by RefSeq, May 2010]

Function:
Monothiol glutaredoxin involved in the biogenesis of iron-sulfur clusters. Required for normal iron homeostasis. Required for normal regulation of hemoglobin synthesis by the iron-sulfur protein ACO1.

Subunit:
Homodimer.

Subcellular Location:
Mitochondrion.

DISEASE:
Defects in GLRX5 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 glutaredoxin family. Monothiol subfamily.
Contains 1 glutaredoxin domain.

SWISS:
Q86SX6

Gene ID:
51218

Database links:

Entrez Gene: 51218 Human

Entrez Gene: 73046 Mouse

Entrez Gene: 362776 Rat

Omim: 609588 Human

SwissProt: Q86SX6 Human

SwissProt: Q80Y14 Mouse

Unigene: 532683 Human

Unigene: 728210 Human

Unigene: 29128 Mouse

Unigene: 104008 Rat



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