ISO 13485:2016 Certified
Category
백인박스(BIB)
1025–1040/1785개 결과 표시
Cat. No. – BS061
Package – 500ml
Storage – RT
Description – 1M Sodium Carbonate Buffer, pH x.x pH adjusted to x.x with Sodium Carbonate and Sodium Bicarbonate. Filtered and Sterile Solution
Cat. No. – BS062
Package – 1000ml
Description – 10mM Sodium Citrate Buffer, pH x.x pH adjusted to x.x with sodium Citrate and Citric acid. Sterile-filtered solution.
Cat. No. – BS063
Storage – Cold
Description – Sodium Chloride 100mM, HEPES, pH 7.4 20mM, EDTA 1mM Ready-to-use Sterile and Filtered Solution
Application – Suitable for molecular biology applications.
Cat. No. – BS064a
Package – 1,000 ml
Description – 5mM Sodium Phosphate Buffer, pH x.x. pH adjusted to x.x with sodium phosphate monobasic and dibasic.
Cat. No. – BS064
Cat. No. – BS065
Storage – RT 15~30℃. Stable for a minimum of 1 years from date of receipt at room temperature
Description – 25mM Sodium Chloride (NaCl) Solution, Sterile and filtered solution. DNase, RNase and Protease none detected.
Cat. No. – BS066
Package – 100ml
Description – The Sodium Bicarbonate Solution is a 0.1M solution, pH 8.3. Filtered and Sterile Solution.
Cat. No. – BS067
Description
Description – Useful substrate for rapid colorimetric assay of N-acetyl-β-glucosaminidase activity in human urine.
Cat. No. – BS069
Package – 10ml
Storage – Freeze
Description – Tris-HCl pH 6.8 250mM, SDS 10%, Glycerol 50%, Bromophenol Blue 0.5%
Cat. No. – BS070
Description –0.1M Sodium Acetate, pH 5.0 pH adjusted to 5.0 with Acetic acid
Cat. No. – BS071
Package – 250ml
Description – 0.5M Sodium borate Buffer, pH x.x
Cat. No. – BS072
Description – 1% Sodium Azide Solution
Cat. No. – BS073
Package – 200ml
Description – Tris-HCl, pH 7.9 50mM, EDTA 10mM, SDS 0.5% * 0.2um Filtered Solution
Cat. No. – BS074
Package –250ml
Description – Tris-HCl, pH 8.8 50mM, Urea 6M, Glycerol 30%, SDS 2%, Bromophenol blue 0.002% Filtered solution
Cat. No. – BS075
Description –2-mercaptoethanol 100 mM, SDS 2%, Tris-HCl, pH6.7 62.5 mM * Efficiency of stripping can be checked by incubating the membrane with chemiluminescent detection reagent.
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