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SLC25A37 (基因名), Mitoferrin-1 (蛋白名), MFRN1_HUMAN.
产品名称:

Human SLC25A37/ Mitoferrin-1 Recombinant Protein

货号:
-
商标:
EIAab®
监管等级:
别名:

Mitochondrial iron transporter 1, Mitochondrial solute carrier protein, Solute carrier family 25 member 37, HT015, MFRN, MSCP

序列号:
Q9NYZ2
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human SLC25A37 Protein
×
Human SLC25A37 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


基因位点
Cytogenetic band: 8p21.2 by HGNC 8p21.2 by Entrez Gene 8p21.2 by Ensembl
SLC25A37 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Mitochondrial iron transporter that specifically mediates iron uptake in developing erythroid cells, thereby playing an essential role in heme biosynthesis. The iron delivered into the mitochondria, presumably as Fe(2+), is then probably delivered to ferrochelatase to catalyze Fe(2+) incorporation into protoprophyrin IX to make heme.


亚细胞位置:
Mitochondrion inner membrane Multi-pass membrane protein


该产品尚未在任何出版物中被引用。

[1].
"Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression."

[2].
"Mitoferrin is essential for erythroid iron assimilation."

[3].
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."

[4].
"Rapid decrease of RNA level of a novel mouse mitochondria solute carrier protein (Mscp) gene at 4-5 weeks of age."

[5].
"Gene expression profiling in the human hypothalamus-pituitary-adrenal axis and full-length cDNA cloning."

[6].
"Genome-wide CRISPR screen identifies HNRNPL as a prostate cancer dependency regulating RNA splicing."

[7].
"Identification of SLC25A37 as a major depressive disorder risk gene."

[8].
"Distinct iron architecture in SF3B1-mutant myelodysplastic syndrome patients is linked to an SLC25A37 splice variant with a retained intron."

[9].
"The mitochondrial transporter family SLC25: identification, properties and physiopathology."

[10].
"Abnormal mitoferrin-1 expression in patients with erythropoietic protoporphyria."
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