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MMEL1 (基因名), Membrane metallo-endopeptidase-like 1 (蛋白名), MMEL1_HUMAN.
产品名称:

Human MMEL1/ Membrane metallo-endopeptidase-like 1 Recombinant Protein
膜metallo-endopeptidase-like 1

货号:

R2033h

商标:
EIAab®
监管等级:
别名:

Membrane metallo-endopeptidase-like 2, NEP2(m), Neprilysin II, Neprilysin-2, NEPII, NEP2, MELL1, MMEL2, NEP2

序列号:
Q495T6
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 MMEL1 Protein
规格 & 价格: cart
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Human MMEL1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 1p36.32 by HGNC 1p36.32 by Entrez Gene 1p36.32 by Ensembl
MMEL1 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:
Metalloprotease involved in sperm function, possibly by modulating the processes of fertilization and early embryonic development. Degrades a broad variety of small peptides with a preference for peptides shorter than 3 kDa containing neutral bulky aliphatic or aromatic amino acid residues. Shares the same substrate specificity with MME and cleaves peptides at the same amide bond.


亚细胞位置:
Membrane Single-pass type II membrane protein Secreted A secreted form produced by proteollytic cleavage also exists.


该产品尚未在任何出版物中被引用。

[1].
"Molecular cloning, tissue distribution, and chromosomal localization of MMEL2, a gene coding for a novel human member of the neutral endopeptidase-24.11 family."

[2].
"Multiple common variants for celiac disease influencing immune gene expression."

[3].
"Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia."

[4].
"Overlap of disease susceptibility loci for rheumatoid arthritis and juvenile idiopathic arthritis."

[5].
"A functionally relevant IRF5 haplotype is associated with reduced risk to Wegener's granulomatosis."

[6].
"Genetic variants in the prediction of rheumatoid arthritis."

[7].
"Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci."

[8].
"Variants at IRF5-TNPO3, 17q12-21 and MMEL1 are associated with primary biliary cirrhosis."

[9].
"Common variants at CD40 and other loci confer risk of rheumatoid arthritis."

[10].
"The DNA sequence and biological annotation of human chromosome 1."
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