MA1-06319

antibody from Invitrogen Antibodies

Targeting: KRT10 CK10, K10, KPP

Western blot (Recommended by provider)

Immunohistochemistry (Data presented on provider website)

Flow cytometry (Recommended by provider)

Other assay (Supportive data in Antibodypedia)

Antibody Data

Product number

MA1-06319

Provider

Invitrogen Antibodies

Product name

Cytokeratin 10 Monoclonal Antibody (RKSE60)

Antibody type

Monoclonal

Antigen

Other

Description

MA1-06319 detects cytokeratin 10 in human, canine, rat, porcine, zebrafish and mouse samples. MA1-06319 has sucessfully been used in Western blotting, flow cytometry, immunocytochemistry, and immunohistochemistry. The MA1-06319 immmunogens are cytokeratins from the human epidermis.  Store at 4ºC or -20ºC if preferred.

Reactivity

Human, Mouse, Rat, Canine, Porcine, Zebrafish

Host

Mouse

Isotype

IgG

Antibody clone number

RKSE60

Vial size

100 µg

Concentration

1 mg/mL

Storage

Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.

References

Submitted references

Loss of FOXC1 contributes to the corneal epithelial fate switch and pathogenesis.

Li M, Zhu L, Liu J, Huang H, Guo H, Wang L, Li L, Gu S, Tan J, Zhong J, Wang B, Mao Z, Fan Y, Liu C, Yuan J, Ouyang H
Signal transduction and targeted therapy 2021 Jan 8;6(1):5

---

Core transcription regulatory circuitry orchestrates corneal epithelial homeostasis.

Li M, Huang H, Li L, He C, Zhu L, Guo H, Wang L, Liu J, Wu S, Liu J, Xu T, Mao Z, Cao N, Zhang K, Lan F, Ding J, Yuan J, Liu Y, Ouyang H
Nature communications 2021 Jan 18;12(1):420

---

Epiboly generates the epidermal basal monolayer and spreads the nascent mammalian skin to enclose the embryonic body.

Panousopoulou E, Hobbs C, Mason I, Green JB, Formstone CJ
Journal of cell science 2016 May 1;129(9):1915-27

Other assay

Supportive validation

Submitted by

Invitrogen Antibodies (provider)

Main image

Experimental details

Fig. 3 Loss of RUNX1 or SMAD3 induces cell identity switch. a Heatmaps of differentially expressed genes produced by RUNX1 or SMAD3 KD. Red mark represents SE-assigned genes. b GO BP analysis for the upregulated genes in RUNX1 -depleted and SMAD3 -depleted LSCs (pvalueCutoff = 0.01 and qvalueCutoff = 0.05). c GSEA for genes that (i) are expressed at higher levels in LSCs than in SESCs and (ii) are more highly expressed in SESCs than in LSCs. NES: normalized enrichment score. d Schema representation of the air-lifting culture system. LSCs were seeded in the transwell inserts and incubated in medium until they were confluent. Then, the medium in the upper chamber was removed to induce differentiation into a stratified epithelium sheet. e Hematoxylin and eosin (H&E) and immunofluorescence staining of the indicated genes in the differentiated corneal epithelium sheet after air-lifting induction. Scale bars, 50 mum. f Immunofluorescence staining of the indicated genes in the differentiated corneal epithelium sheets treated with the indicated shRNAs. Scale bar, 50 mum.

Supportive validation

Submitted by

Invitrogen Antibodies (provider)

Main image

Experimental details

Fig. 6 Pathological changes of corneal epithelium. H&E staining and immunofluorescence analysis of the indicated genes in corneal inflammatory (47 years old, female), ulcer (62 years old, female), alkali burn (33 years old, male), and leukoma (51 years old, female) tissues. Scale bars, 200 mum.