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SRP4210

Sigma-Aldrich

GRO/KC from mouse

recombinant, expressed in E. coli, ≥98% (SDS-PAGE), ≥98% (HPLC)

Synonym(s):

CXCL1, GRO α, GRO1, Growth-regulated α protein, NAP-3

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About This Item

MDL number:
UNSPSC Code:
12352202
NACRES:
NA.32

Pricing and availability is not currently available.

biological source

mouse

recombinant

expressed in E. coli

Assay

≥98% (HPLC)
≥98% (SDS-PAGE)

form

lyophilized

potency

10-100 ng/mL

mol wt

~7.8 kDa

packaging

pkg of 20 μg

impurities

endotoxin, tested

NCBI accession no.

UniProt accession no.

General description

Growth-regulated oncogenes (GRO)/keratinocyte chemoattractant (KC) belongs to the growing inflammatory protein superfamily. KC is characterized with four conserved cysteine residues with a CXC motif.[1]
Mouse KC (also known as mouse GRO-α) belongs to the C-X-C family of chemokines. Mouse KC is a 7.8 kDa protein containing 72 amino acid residues.

Biochem/physiol Actions

Growth-regulated oncogenes (GRO)/keratinocyte chemoattractant (KC) plays a vital role in wound healing and inflammation.[2] In rat, serum levels of GRO/KC can be used as a predictive biomarker for inhibitory effect of chemopreventive agents on esophageal carcinogenesis.[3]

Physical form

Sterile filtered and then lyophilized without any additives.

Reconstitution

Centrifuge the vial prior to opening. Avoid freeze-thaw cycles.
Reconstitute in water to a concentration of 0.1-1 mg/mL. This solution can be diluted into other aqueous buffers.

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Cloning and sequencing of a new gro transcript from activated human monocytes: expression in leukocytes and wound tissue
Iida NAOKO and Grotendorst GR
Molecular Cell Biology, 10(10), 5596-5599 (1990)
Cloning and sequencing of a new gro transcript from activated human monocytes: expression in leukocytes and wound tissue.
Iida N A O K O, et al.
Molecular and Cellular Biochemistry, 10(10), 5596-5599 (1990)
Multiple berry types prevent N-nitrosomethylbenzylamine-induced esophageal cancer in rats
Stoner GD, et al.
Pharmaceutical Research, 27(6), 1138-1145 (2010)
Aimalie L Hardaway et al.
Clinical & experimental metastasis, 32(4), 353-368 (2015-03-25)
Increased bone marrow adiposity is a common feature of advanced age, obesity and associated metabolic pathologies. Augmented numbers of marrow adipocytes positively correlate with dysregulated bone remodeling, also a well-established complication of metastatic disease. We have shown previously that marrow
Yuan Sun et al.
The journal of pain : official journal of the American Pain Society, 15(8), 856-866 (2014-06-03)
Chronic opioid consumption increases postoperative pain. Epigenetic changes related to chronic opioid use and surgical incision may be partially responsible for this enhancement. The CXCL1/CXCR2 signaling pathway, implicated in several pain models, is known to be epigenetically regulated via histone

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