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p47phox-pK [Clone C, clone K, p47]
p47phox-pK [Clone C, clone K, p47]
規格:
貨期:
編號:B213674
品牌:Mingzhoubio

標準菌株
定量菌液
DNA
RNA

規格:
凍干粉
斜面
甘油
平板


產品名稱 p47phox-pK [Clone C, clone K, p47]
商品貨號 B213674
Designations p47phox-pK [Clone C, clone K, p47]
GenBank Number

M26193

Species Homo sapiens, human
Applications
produces protein neutrophil cytosolic factor 1 (47kD, chronic granulomatous disease, autosomal 1) neutrophil cytosolic factor 1
Vector
Construct size (kb): 4.300000190734863
Insert
DNA: cDNA
Insert lengths(kb): 1.350000023841858
Tissue: HL-60 cell line (DMSO induced)
Gene product: neutrophil cytosolic factor 1 (47kD, chronic granulomatous disease, autosomal 1)(neutrophil cytosolic factor 1) [NCF1]
Target Gene: neutrophil cytosolic factor 1 (47kD, chronic granulomatous disease, autosomal 1)
Insert Size (kb) 1.350
Biosafety Level 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Shipping Information Distributed: DNA (dried). Rehydrate with TE. (amount: 2 ug)
Comments
Restriction digests of the clone give the following sizes (kb): BamHI--3.7, 0.64; EcoRI--3.0, 1.35; HindIII--4.4; PstI--3.3, 0.5, 0.27; XbaI--4.4.
The insert contains the following restriction sites (nt from the 5' EcoRI site): XmnI--72, AccI--142, BglII--159, PstI--318; BamHI--634; NarI--916; SmaI--1060.
This clone encodes the synthesis of a 50 kDa fusion protein recognized by anti-NADPH oxidase antisera.
Detects a mRNA of 1.4 kb.
References

Volpp BD, et al. Cloning of the cDNA and functional expression of the 47-kilodalton cytosolic component of human neutrophil respiratory burst oxidase. Proc. Natl. Acad. Sci. USA 86: 7195-7199, 1989. PubMed: 2550933

Volpp BD, et al. Two cytosolic neutrophil oxidase components absent in autosomal chronic granulomatous disease. Science 242: 1295-1297, 1988. PubMed: 2848318

. Medical sciences: correction. Proc. Natl. Acad. Sci. USA 86: 9563, 1989.

Casimir CM, et al. Autosomal recessive chronic granulomatous disease caused by deletion at a dinucleotide repeat. Proc. Natl. Acad. Sci. USA 88: 2753-2757, 1991. PubMed: 2011585

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