Erratum to “Phospholipase A2 expression in human and rodent insulin-secreting cells” [Mol. Cell. Endocrinol. 112 (1995) 177–183]

t?eru’ara E ellular

ndocrinology

ELSEVIER

Molecular and Cellular Endocrinology 114 (1995) 227-228

Erratum

Erratum to “Phospholipase A, expression in human and rodent insulin-secreting cells” [Mol. Cell. Endocrinol. 112 (1995) 177-183]’ A.C. Loweth”, J.H.B. Scarpellob, N.G. Morgan”” aDepartment of Biological Sciences, Cellular Pharmacology Group, Keele Uniwrsity, Keele, Staffordrhire, ST5 5BG, UK bDepartment of Medicine, Cellular Phammology Group, Keele Uniwrsity Keele, Staffordshire, STY5BG, UK

Received 23 January 1995; accepted 24 May 1995

The publisher wishes to point out that the lanes indicated as 100 kDA were incorrect in Figs. 1 and 2 of this article. A corrected version of both Figs. 1 and 2 are reproduced here.

a

b

C

d

a

b

C

d

Fig. 1. Probing of pancreatic islet cell proteins with anti-cPL4, serum. (A) Gels were loaded with: lane (a) 50 pg U937 cytosol; lane (bl30 Kg rat kidney cytosol; lane (c) 100 pg rat pancreas cytosol; lane (d) 100 kg rat islet homogenate. (B) Lane (a) SO Fg human islet cytosol; lane (b) 250 pg RINm5F cytosol; lane (c) 250 pg HIT-T15 cytosol; lane (d) 50 pg U937 homogenate. Fractions were electrophoresed in parallel with molecular weight markers, blotted onto PVDF membrane and probed with anti-cPLA2-serum cl:1200 dilution). Immunoreactive proteins were visualised by chemiluminescence detection. The molecular weights &Da) of the major protein bands are shown.

‘SSDI of original article: 0303-7207 (95) 03595-X 0303-7207/95/$09.50 SSDI

0 1995 Elsevier Science Ireland Ltd. All rights reserved.

0303-7207(95)03686-2

Molecular and Cellular Endocrinology 114 (1995) 227-228

228

c

d

1OOkDa

Fig. 2. Cross-reactivity of cPLA, antiserum with the enzyme expressed in cytosol; lane (bl 100 pg rat islet homogenate; lanes (cl, cd), (e) and (f) 25, electrophoresed in parallel with molecular weight markers, blotted onto dilution). Immunoreactive proteins were visualised by chemiluminescence protein bands are shown.

rat tissue. Gels were loaded with: lanes (a) and (gl 50 pg U937 45, 60 and 90 Fg rat kidney cytosol, respectively. Fractions were PVDF membrane and probed with anti-cPLA&erum (1:1200 detection. The apparent molecular weights &Da) of the major

Also throughout the article ‘mg’ must be corrected to read ‘pg’.