rapid hybridization buffer Search Results


rapid hyb buffer  (Cytiva Europe)
95
Cytiva Europe rapid hyb buffer
Rapid Hyb Buffer, supplied by Cytiva Europe, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rapid hyb buffer  (Amersham Life Sciences Inc)
86
Amersham Life Sciences Inc rapid hyb buffer
Rapid Hyb Buffer, supplied by Amersham Life Sciences Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rapid hybridization solution  (TaKaRa)
95
TaKaRa rapid hybridization solution
Rapid Hybridization Solution, supplied by TaKaRa, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/ExpressHyb+Hybridization+Solution/us08377645-167-4-7
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hcc rapid hybridization solution  (Amersham Life Sciences Inc)
86
Amersham Life Sciences Inc hcc rapid hybridization solution
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Hcc Rapid Hybridization Solution, supplied by Amersham Life Sciences Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/hybridization+rapid+solution/10__1002_slash_hep__510240206-58-17-21
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rapid hyb buffer  (GE Healthcare)
95
GE Healthcare rapid hyb buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hyb Buffer, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/Rapid-hyb+Buffer+sufficient+for+4000+cm%C2%B2+membrane/pmc07156407-345-6-9
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amersham hybridization buffer  (GE Healthcare)
86
GE Healthcare amersham hybridization buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Amersham Hybridization Buffer, supplied by GE Healthcare, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/Amersham+ECL+Gold+Hybridization+Buffer+sufficient+for+4000+cm%C2%B2/pmc01400569-302-5-10
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4000 × g  (Danaher Inc)
99
Danaher Inc 4000 × g
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
4000 × G, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/Filter/10__5433_slash_1679___0359__2017v38n4p1841-66-23-36
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4000 × g - by Bioz Stars, 2026-11
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rapid hyb buffer  (Amersham Pharmacia Biotech Ltd)
86
Amersham Pharmacia Biotech Ltd rapid hyb buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hyb Buffer, supplied by Amersham Pharmacia Biotech Ltd, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/buffer+hyb+rapid/pm16207730-184-9-11
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rapid-hyb buffer  (Buchler GmbH)
90
Buchler GmbH rapid-hyb buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hyb Buffer, supplied by Buchler GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/rapid+hyb+buffer/pm08995369-46-11-14
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rapid hybridization buffer  (TaKaRa)
97
TaKaRa rapid hybridization buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hybridization Buffer, supplied by TaKaRa, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/Lysis+Buffer/pm16153868-303-5-8
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rapid-hyb solution  (Becton Dickinson)
90
Becton Dickinson rapid-hyb solution
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hyb Solution, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/rapid+hybridization+buffer/rapid+hyb+solution/pm17637750-282-5-7
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rapid-hyb buffer  (Becton Dickinson)
90
Becton Dickinson rapid-hyb buffer
FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with <t>HCC.</t> Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. <t>Hybridization</t> was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.
Rapid Hyb Buffer, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with HCC. Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. Hybridization was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.

Journal: Hepatology

Article Title: Overexpression of matrix metalloproteinase 9 gene in hepatocellular carcinoma with invasive potential

doi: 10.1002/hep.510240206

Figure Lengend Snippet: FIG. 1. (A) Northern blot analysis of MMP-9 mRNA expression in liver tissues with HCC. Five micrograms of poly (A)/ RNA from each human tissue was used in the Northern blot analysis. Hybridization was per- formed with human MMP-9 comple- mentary DNA. The 2.8-kilobase band, corresponding to the MMP-9 transcript, was detected. S26r mRNA expression is shown as the corre- sponding internal control in the lower panel. N, nontumorous portion; T, tu- morous portion; and C, portion adja- cent to the capsule. (B) Northern blot analysis of MMP-9 mRNA expression (upper panel) and of corresponding TIMP-1 mRNA expression (middle panel) in liver tissues with HCC. Hy- bridization was performed, as de- scribed in Materials and Methods. Five micrograms of poly (A)/ RNA was loaded into each slot. The 0.9- kilobase TIMP-1 transcript was de- tected in tumorous tissues, in nontu- morous tissues, and in the portions of the tumors adjacent to the capsules. S26r mRNA expression is shown as the corresponding control in the lower panel. N, nontumorous portion; T, tumorous portion; and C, portion adjacent to the capsule.

Article Snippet: Hybridization was performed at 657C for 2 hours in analysis, tumorous and adjacent nontumorous tissues from 14 HCC Rapid Hybridization Solution (Amersham) with labeled probe.

Techniques: Northern Blot, Expressing, Hybridization, Control, Capsules

FIG. 2. Northern blot analysis of MMP-2 mRNA expression (upper panel) and of corresponding TIMP-2 mRNA expression (middle panel) in liver tissues with HCC. 5 mg of poly (A)/ RNA from each human tissue and 10 mg of total RNA from T98G (a glioblastoma cell line as a positive control) were used in Northern blot analysis. Hybridization was per- formed, as described in Materials and Methods. The 3.1 kilobase MMP-2 transcript and TIMP-2 transcripts of 3.5 and 1.0 kilobase were detected in both tumorous and nontumorous liver tissues from HCC patients. Lower lanes show S26r mRNA ex- pression corresponding to each of the upper lanes. N, nontumorous portion; and T, tumorous portion.

Journal: Hepatology

Article Title: Overexpression of matrix metalloproteinase 9 gene in hepatocellular carcinoma with invasive potential

doi: 10.1002/hep.510240206

Figure Lengend Snippet: FIG. 2. Northern blot analysis of MMP-2 mRNA expression (upper panel) and of corresponding TIMP-2 mRNA expression (middle panel) in liver tissues with HCC. 5 mg of poly (A)/ RNA from each human tissue and 10 mg of total RNA from T98G (a glioblastoma cell line as a positive control) were used in Northern blot analysis. Hybridization was per- formed, as described in Materials and Methods. The 3.1 kilobase MMP-2 transcript and TIMP-2 transcripts of 3.5 and 1.0 kilobase were detected in both tumorous and nontumorous liver tissues from HCC patients. Lower lanes show S26r mRNA ex- pression corresponding to each of the upper lanes. N, nontumorous portion; and T, tumorous portion.

Article Snippet: Hybridization was performed at 657C for 2 hours in analysis, tumorous and adjacent nontumorous tissues from 14 HCC Rapid Hybridization Solution (Amersham) with labeled probe.

Techniques: Northern Blot, Expressing, Positive Control, Hybridization