KLENOW ENZYME
货号： PF059-.08ML 产品名称： KLENOW ENZYME 品牌： Merck 规格： *** 3周到货 生化实验
Klenow Enzyme
This product has been discontinued.
The large fragment of DNA polymerase I. The Klenow fragment exhibits 5′ to 3′ DNA polymerase and 3′ to 5′ exonuclease activity, but lacks the 5′ to 3′ exonuclease activity of intact DNA polymerase I.
产品信息
Form Liquid
Formulation In 50 mM potassium phosphate buffer, 0.25 mM dithiothreitol, 50% glycerol, pH 7.0.
Preservative None
Avoid freeze/thaw 是的
Unit definition One unit is the amount of enzyme required to incorporate 10 nmol of total nucleotide into acid-insoluble form in 30 min at 37°C.
商店和运输信息
Storage -20°C
Ship Dry Ice Only
Standard Handling
-20°C
PF060-.155ML TDT ENZYME 品牌 Merck
TDT ENZYME
货号： PF060-.155ML 产品名称： TDT ENZYME 品牌： Merck 规格： *** 3周到货 生化实验
TdT, Calf Thymus
Terminal Deoxynucleotidyl Transferase
Native TdT from calf thymus. Tdt is a DNA polymerase that catalyzes the addition of deoxynucleotides to the 3′ hydroxy terminus of either double of single stranded DNA in a template-independent manner.
产品信息
Form Liquid
Formulation 775 Units in 50 mM potassium phosphate buffer, 1 mM B-mercaptoethanol, 50% glycerol, pH 7.2.
Preservative None
Applications
DNA Labeling
Avoid freeze/thaw 是的
Unit definition One unit is the amount of enzyme required to transfer 1 nmol of dAMP from dATP to the 3′-OH terminus of d(A)50 in 60 min at 37°C.
商店和运输信息
Storage -20°C
Ship Dry Ice Only
Standard Handling
-20°C
QIA55-1EA MMP-1 ELISA 品牌 Merck
MMP-1 ELISA
货号： QIA55-1EA 产品名称： MMP-1 ELISA 品牌： Merck 规格： *** 3周到货 生化实验
MMP-1 ELISA Kit
The MMP-1 ELISA is a non-isotopic colorimetric assay kit for the in vitro quantification of human MMP-1 protein in tissue culture medium and serum.
产品信息
Format 96-well plate
Form 96 Tests
Detection method Colorimetric
Species reactivity human
Avoid freeze/thaw 是的
Specificity Human pro-MMP-1 and recombinant MMP-1
Sensitivity 0.023 ng/ml
Assay range 0.023 – 3.6 ng/ml
Assay time 3.5 h
Sample type Tissue culture medium or human serum
Kit contains 96-Well Coated Plate, Human pro-MMP-1 Standard, HRP Conjugated Detector Antibody, Assay Buffers, Diluents, Color Reagent, Stop Solution, Plate Cover, and a user protocol.
Declaration Manufactured by Daiichi Fine Chemical Co., Ltd. Not available for sale in Japan.
商店和运输信息
Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping chargesmay be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Storage -20°C
Ship Dry Ice Only
Multiple Toxicity Values, refer to MSDS
-20°C
69036-8000UN FACTOR Xa 品牌 Merck
FACTOR Xa
货号： 69036-8000UN 产品名称： FACTOR Xa 品牌： Merck 规格： *** 3周到货 生化实验
Factor Xa, Restriction Grade, Bovine Plasma
Restriction Grade Factor Xa is a highly purified preparation isoated from bovine plasma and activated with Russell’s viper venom. This preparation is purified to near homogeneity and shows
no secondary cleavage from contaminating proteases. The preparation is also functionally tested for activity with fusion proteins. Like enterokinase, Factor Xa cleaves at the C-terminal side
of the recognition sequence (IleGluGlyArg↓) and can therefore be used for removing all vector-encoded sequences from appropriately designed constructs.
Specific Activity: ≥150 IU/mg
One IU isdefined as the amount of enzyme that will release 1 µmole of p-nitroaniline per minute using methanesulfonyl-D-leucyl-glycyl-arginyl-paranitroanilide at 37°C, pH 8.4.
One µg of enzyme cleaves 50 µg Cleavage Control Protein to >95% completion in 16 hr at 25°C in a buffer containing 50 mM Tris-HCl pH 8.0, 100 mM NaCl, and 5 mM CaCl2.
产品信息
Avoid freeze/thaw 是的
Biological activity One microgram of enzyme cleaves 50 µg Xa Cleavage Control Protein to >95% completion in 16 hours at 25°C in a buffer containing 50 mM Tris-HCl pH 8.0, 100 mM NaCl, and 5
mM CaCl2.
Components
• 100 µg Restriction Grade Factor Xa
• 2 ml Factor Xa Dilution/Storage Buffer
• 1 ml 10X Factor Xa Cleavage Buffer
• 10 µg Cleavage Control Protein
商店和运输信息
Storage -20°C
Ship Blue Ice Only
Multiple Toxicity Values, refer to MSDS
-20°C
114825-25MG Adapalene 品牌 Merck
Adapalene
货号： 114825-25MG 产品名称： Adapalene 品牌： Merck 规格： *** 3周到货 生化实验
Adapalene
CD 271, Differin, 6-(3-(1-Adamantyl)-4-methoxyphenyl)-2-naphthoic acid, CD271, RAR Agonist V, ADA
A cell-permeable naphthoic acid compound that exhibits selective affinity and agonistic potency toward RARβ and RARγ over RARα (Kd = 34, 130, and 1100 nM, respectively; AC50 = 2.3, 9.3, and 22 nM, respectively, in COS-7-based reporter assays) without appreciable affinity toward cytosolic retinoic acid binding proteins CRABP I/II (Kd >> 1 µM) or detectable activity toward RXRα (AC50 > 1 µM). The biological activity and pharmaceutical efficacy of ADA are generally shown to be superior to those of ATRA/Tretinoin (Cat. No. 554720) both in vitro and in vivo.
产品信息
Form White solid
Molar mass 412.5
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥97% by HPLC
Solubility DMSO
Chemical formula C28H28O3
CAS number 106685-40-9
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
197226-10MG BCRP Inhbitor 品牌 Merck
BCRP Inhbitor
货号： 197226-10MG 产品名称： BCRP Inhbitor 品牌： Merck 规格： *** 3周到货 生化实验
BCRP Inhbitor
N-(4-(2-hydroxyethyl)phenyl)-2-(4-nitrobenzamido)benzamide
A non-tetrahydroisoquinoline BCRP specific inhibitor based on the anthranilic acid scaffold, that displays an IC50 of 1.39 µM in a Hoechst 33343 assay in stably transfected MDCK BCRP cells, which is ˜50-fold more potent than novobiocin (IC50 = 65 µM), and shows no effect towards other ATP binding cassette (ABC) transporters P-gp and MRP1 at up to a concentration of 10 µM. It is shown to be an allosteric inhibitor in enzyme kinetics assays in the presence of BCRP specific substrates pheophorbide A and imitanib, and does not lead to a decrease in cell viability up to a concentration of 10 µM.
产品信息
Form Off-white solid
Molar mass 405.4
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C22H19N3O5
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
200980-25MG Bikinin 品牌 Merck
Bikinin
货号： 200980-25MG 产品名称： Bikinin 品牌： Merck 规格： *** 3周到货 生化实验
Bikinin
4-((5-Bromo-2-pyridinyl)amino)-4-oxobutanoic acid, Arabidopsis GSK-3 Inhibitor, Arabidopsis SHAGGY-related Kinase Inhibitor, GSK-3-like Kinase BIN2 Inhibitor
A cell-permeable nonsteroidal pyridinylamido compound that acts as an ATP-competitive inhibitor against 7 of the 10 Arabidopsis thaliana GSK3’s, BIN2 & ASKα/ γ/ε/ζ/ι/θ, but not ASKβ/δ or three other Arabidopsis Ser/Thr kinases, AtMPK4, AtMPK6, and AtAURORA1. The inhibitory activity is plant species-selective, as Bikinin exhibits much reduced activity against human Gsk-3β, Aurora B, Aurora C (45.6%, 69.4%, and 42.8% inhibition, respectively, with 10 µM Bikinin), and little or no activity against 74 other human kinases, nor does it affect GSK-3β-mediated dorsoventral axis formation during Xenopus embryo development. Bikinin at 30 µM is shown to bypass brassinolide (BL) and BRI1 and effectively activate brassinosteroid (BR) signaling responses in Arabidopsis thaliana seedings, including decreased BES1 phosphorylation, increased hypocotyl length, long and bending petioles, blade-shaped, pale-green leaves, as well as reduced lateral root density.
产品信息
Form White solid
Molar mass 273.1
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥90% by HPLC
Solubility DMSO
Chemical formula C9H9BrN2O3
CAS number 188011-69-0
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
204001-10MG BX-795 品牌 Merck
BX-795
货号： 204001-10MG 产品名称： BX-795 品牌： Merck 规格： *** 3周到货 生化实验
BX-795
N-(3-((5-Iodo-4-((3-(2-thienylcarbonyl)amino)propyl)amino)-2-pyrimidinyl)amino)phenyl)-1-pyrrolidinecarboxamide, Aurora Kinase Inhibitor VIII, AMPK Related Kinase 5 Inhibitor I, ARK5 Inhibitor I, NUAK Kinase Inhibitor I, NUAK1 Inhibitor I, SnF1 Like Kinase-1 Inhibitor I
A cell-permeable aminopyrimidine compound that acts as a potent, ATP-competitive and reversible multi-kinase inhibitor (IC50 = 11 nM for PDK1 at ≤ 10 µM of ATP; IC50 = 5 , 6, 19, 31, 41 and 111 nM for NUAK1, TBK1, MARK4, Aurora B, IKKε and PDK1 at 100 µM of ATP, respectively) and displays 50-fold greater selectivity over Cdk2/E, EGFR, GSK-3β, IR, c-Kit, PKA, PKC, TAK1 and VEGFR. Shown to block PDK1/Akt signaling, induce growth arrest and apoptosis in PC-3 and MDA-468 cells (IC50 = 0.25 and 0.75 µM, respectively); further, inhibit phosphorylation (pSer396), nuclear translocation and transcriptional activity of IRF3 and reduce IFN-β production in stimulated macrophages.
产品信息
Form Pale yellow solid
Molar mass 591.5
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C23H26IN7O2S
CAS number 702675-74-9
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
239836-10MG Cyclophilin A Inhibitor 品牌 Merck
Cyclophilin A Inhibitor
货号： 239836-10MG 产品名称： Cyclophilin A Inhibitor 品牌： Merck 规格： *** 3周到货 生化实验
Cyclophilin A Inhibitor
Acts as an inhibitor of cyclophilin A (IC50 = 1.5nM), which is approximately 27 times more potent than that of Cyclosporin A, in in vitro assays.
产品信息
Form Off-white solid
Molar mass 380.8
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C21H14ClFN2O2
CAS number 1186372-20-2
商店和运输信息
Storage -20°C
Ship Ambient Temperature Only
Standard Handling
-20°C
324377-50MG Donepezil Hydrochloride 品牌 Merck
Donepezil Hydrochloride
货号： 324377-50MG 产品名称： Donepezil Hydrochloride 品牌： Merck 规格： *** 3周到货 生化实验
Donepezil Hydrochloride
A brain-penetrating, reversible, and selective piperidine acetylcholinesterase inhibitor with an IC50 = 5.7 nM in vitro, and a 1250-fold selectivity over butylcholinesterase. In vivo, there is a marked and significant increase in acetylcholine content in rat cerebral cortex at a p.o. dose of 5 mg/kg. Furthermore, it inhibits brain cholinesterase (ChE) dose-dependently (ID50 = 2.6 mg/kg) without any marked adverse effects on ChE in the heart and small intestine. In a clinical trial, it has been shown to reduce AChE activity by 63.7% for the 5mg/d group and 77.3% for the 10mg/d group in Alzheimer’s disease patients. Its off-target effects are indicated with the reversibly of inhibited voltage-gated K+/Na+ channels.
产品信息
Form White solid
Molar mass 415.95
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥98% by HPLC
Solubility H2O
Chemical formula C24H29NO3HCl
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
324521-25MG Eeyarestatin I 品牌 Merck
Eeyarestatin I
货号： 324521-25MG 产品名称： Eeyarestatin I 品牌： Merck 规格： *** 3周到货 生化实验
Eeyarestatin I
ES1, 1-(4-Chloro-phenyl)-3-(3-(4-chloro-phenyl)-5,5-dimethyl-1-(3-(5-nitro-furan-2-yl)-allyldiene-hydrazinocarbonylmethyl)-2-oxo-imidazolidin-4-yl)-1-hydroxyl-urea, EerI, ERAD Inhibitor II, p97 Inhibitor II, Valosin-containing Protein Inhibitor II, VCP Inhibitor II
A cell-permeable oxo-imidazolidinyl-hydroxyurea that preferentially localizes to ER, where it interacts with AAA (ATPase associated with diverse cellular activities) ATPase p97 (Kd = 5 – 10 µM) via its nitrofuran-containing moiety, without exhibiting affinity toward Hsp70 or AAA ATPase NSF (N-methylmaleimide-sensitive factor). Evidence indicates that EerI cellular metabolite, but not EerI itself, is responsible for the inhibition of ER membrane translocon sec61 complex-mediated transfer of newly synthesized polypeptide, resulting in a blockage of ER-mediated posttranslational glycosylation and signal peptide removal (Effective conc. = 8 µM in HepG2 and HeLa cultures). Ether independent or as a consequence of the early effect on sec61 complex, EerI culture treatment also induces a selective dissociation of an 180 kDa protein from the atx3-containing p97/VCP (Valosin-containing protein) complex and a blockage of the complex-associated deubiquitination of ERAD (ER-associated protein degradation) substrates in a reversible manner, resulting in an accumulation of polyubiquitinated proteins (Effective conc. = 10 µM in A9 and 293T cultures). EerI culture treatment (10 µM) is also demonstrated to selectively induce cytotoxicity in lymphoid cell lines, BJAB, HBL-2, JEKO-1, Jurkat, KMS-12, MINO, as well as primary leukemia cells from CLL (chronic lymphocytic leukemia) patients, but not PBMC from healthy donors, by upregulating the BH3-only pro-apoptotic protein NOXA in cancer cells via ATF3/4 activation and a downregulation of H2A ubiquitination. Unlike DBeQ (Cat. No. 506190), EeRI does not inhibit p97 ATPase activity.
产品信息
Form Light yellow-orange solid
Molar mass 630.4
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥90% by HPLC
Solubility DMSO
Chemical formula C27H25Cl2N7O7
CAS number 412960-54-4
商店和运输信息
Storage +2°C to +8°C
Ship Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Standard Handling
2°C – 8°C
341329-25MG Fatostatin 品牌 Merck
Fatostatin
货号： 341329-25MG 产品名称： Fatostatin 品牌： Merck 规格： *** 3周到货 生化实验
Fatostatin
A cell-permeable diarylthiazole compound that prevents the cellular activation of the SREBP-1/2 (Sterol Regulatory Element Binding Proteins 1/2) precursors to the active nuclear forms (>95% inhibition at 20 µM in CHO-K1 cells) by blocking SREBPs-SCAP (SREBP Cleavage-Activating Protein) ER to Golgi translocation with little effect against the transcription activity of the mature SREBPs. Binding studies employing recombinant SCAP truncation constructs reveal that Fatostatin targets SCAP between aa 448 to 767 in a reversible manner and is of no effect against SREBP-SCAP interaction. Fatostatin effectively suppresses SREBPs-dependent cellular functions in vitro, such as insulin-induced 3T3-L1 adipogenesis (complete inhibition at ≤20 µg/ml) and IGF1-dependent DU-145 proliferation (IC50 = 100 nM), and exhibits in vivo efficacy in lowering blood glucose level (by 70%) and body weight (by 12%) of ob/ob mice over a 28-day treatment period (30 mg/kg daily i.p.) without affecting animal food intake or apparent adverse effects.
产品信息
Form Pale yellow solid
Molar mass 375.3
Protect from Light 是的
Hygrocopic 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C18H18N2S • HBr
CAS number 298197-04-3
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
375680-5MG Hesperadin 品牌 Merck
Hesperadin
货号： 375680-5MG 产品名称： Hesperadin 品牌： Merck 规格： *** 3周到货 生化实验
Hesperadin
A cell-permeable indolinone compound that interacts with both the ATP- and the adjacent hydrophobic binding pocket of Aurora B and acts as a rapid and reversible inhibitor of Aurora kinase B activity (IC50 ~ 250 nM) with moderate selectivity over Cdk1/B, Cdk2/E and Cdk4/D1 (IC50 = 1.2, > 10 and > 10 µM). Also, potently inhibits several kinases at 1 µM in a 25-kinase screening panel (100%, 100%, 96%, 88%, 87% and 84% against Lck, PHK, AMPK, MKK1, MAPKAP-K1 and Chk1, respectively). Reported to reduce histone H3-Ser10 phosphorylation, inhibit cytokinesis, promote chromosome biorientation, perturb mitosis and polyploidy in mammalian cells.
产品信息
Form Yellow solid
Molar mass 516.7
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C29H32N4O3S
CAS number 422513-13-1
商店和运输信息
Storage -20°C
Ship Shipped at Ambient Temperature or with Blue Ice or with Dry Ice
Regulatory Review
-20°C
382111-10MG HistoneAcetyltransferaseInhibitorIVCPTH2 品牌 Merck
HistoneAcetyltransferaseInhibitorIVCPTH2
货号： 382111-10MG 产品名称： HistoneAcetyltransferaseInhibitorIVCPTH2 品牌： Merck 规格： *** 3周到货 生化实验
Histone Acetyltransferase Inhibitor IV, CPTH2
A cell-permeable thiazolyl-hydrazone compound that inhibits the acetylation of histone H3 by recombinant human Gcn5 in a substrate-competive manner, while exhibiting little activity against rhGcn5 autoacetylation. Although functional knockout of Gcn5 in Saccharomyces cerevisiae by genetic deletion or by CPTH2 treatment is not detrimental to the survival of the budding yeast, CPTH2 treatment is shown to inhibit the growth of yeast strain genetically deleted of Gcn5, but not strains deleted of Elp3 or Sas2.
产品信息
Form Brown solid
Molar mass 291.8
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C14H14ClN3S
CAS number 357649-93-5
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
401010-5MG I-BET 品牌 Merck
I-BET
货号： 401010-5MG 产品名称： I-BET 品牌： Merck 规格： *** 3周到货 生化实验
I-BET
Form Yellowish white solid
Molar mass 423.9
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥98% by Chiral HPLC
Solubility DMSO
Chemical formula C22H22ClN5O2
商店和运输信息
Storage -20°C
Ship Shipped with Blue Ice or with Dry Ice
Regulatory Review
-20°C
401011-500UG Hypothemycin 品牌 Merck
Hypothemycin
货号： 401011-500UG 产品名称： Hypothemycin 品牌： Merck 规格： *** 3周到货 生化实验
Hypothemycin
Form Lyophilized solid
Molar mass 378.4
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥97% by HPLC
Solubility DMSO
Chemical formula C19H22O8
CAS number 76958-67-3
商店和运输信息
Storage -20°C
Ship Shipped with Blue Ice or with Dry Ice
Standard Handling
-20°C
401251-10MG IM-412 品牌 Merck
IM-412
货号： 401251-10MG 产品名称： IM-412 品牌： Merck 规格： *** 3周到货 生化实验
IM-412
3-(2-chlorobenzyl)-1,7-dimethyl-1H-imidazo[2,1-f]purine-2,4(3H,8H)-dione, TGF beta Inhibitor, IM-412
Form Off-white solid
Molar mass 343.77
Purity ≥90% by HPLC
Solubility DMSO or EtOH
Chemical formula C16H14ClN5O2
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Standard Handling
2°C – 8°C
438193-5MG LRRK2-IN-1 品牌 Merck
LRRK2-IN-1
货号： 438193-5MG 产品名称： LRRK2-IN-1 品牌： Merck 规格： *** 3周到货 生化实验
LRRK2-IN-1
Form Yellow-white to pale yellow powder
Molar mass 570.31
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥95% by HPLC
Solubility DMSO
Chemical formula C31H38N8O3
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Regulatory Review
2°C – 8°C
445820-5MG Meriolin 2 品牌 Merck
Meriolin 2
货号： 445820-5MG 产品名称： Meriolin 2 品牌： Merck 规格： *** 3周到货 生化实验
Meriolin 2
3-((2-Amino)pyrimidin-4-yl)-4-hydroxy-1H-pyrrolo[2,3-b]pyridine
A cell-permeable, ATP-binding site-targeting azaindolopyrimidine compound that inhibits against Cdk2/A, Cdk9/T, DYRK1A, Cdk5/p25, CK1δ/ε, Cdk1/B, and GSK-3α/β kinase activity (IC50 = 18, 18, 35, 50, 50, 57, and 500 nM, respectively). Shown to induce DEVDase activity in SH-SY5Y neuroblastoma cultures (by 5.46-fold in 24 h at 1 µM) and exhibit antiproliferative activity toward SH-SY5Y, multiple myeloma KMS-11, human embryonic kidney HEK293, colorectal adenocarcinoma LS 174T, and glioma GBM cells in vitro (IC50 = 0.41, 0.6, 0.96, 1.06, and 1.21 µM, respectively).
产品信息
Form Yellow solid
Molar mass 227.2
Protect from Light 是的
Packaged under inert gas 是的
Purity ≥93% by HPLC
Solubility DMSO
Chemical formula C11H9N5O
商店和运输信息
Storage +2°C to +8°C
Ship Ambient Temperature Only
Regulatory Reviewg
2°C – 8°C
454126-100MG Methotrexate 品牌 Merck
Methotrexate
货号： 454126-100MG 产品名称： Methotrexate 品牌： Merck 规格： *** 3周到货 生化实验
Methotrexate
Inhibits thymidylate synthetase, is a nonselective de novo purine synthesis inhibitor, and has a significant toxicity profile including hepatotoxicity, pneumonitis, and bone marrow suppression. Potent folic acid antagonist. Induces apoptosis in HL-60 human leukemia cells. Also useful as an antitumor agent.
产品信息
Form Yellow solid
Molar mass 508.5
Protect from Light 是的
Purity ≥98% by HPLC
Solubility DMSO
Chemical formula C20H22N8O5 • 3H2O
CAS number 59-05-2
Merck USA index 14, 5985
商店和运输信息
Hazardous Materials Attention: Due to the nature of the Hazardous Materials in this shipment, additional shipping chargesmay be applied to your order. Certain sizes may be exempt from the additional hazardous materials shipping charges. Please contact your local sales office for more information regarding these charges.
Storage +2°C to +8°C
Ship Ambient Temperature Only
Toxic
2°C – 8°C