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Ace+Method+Development+Kits


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Supplier:  TCI America
Description:   CAS Number: 2491-06-7
MDL Number: MFCD00012610
Molecular Formula: C4H9NO2
Molecular Weight: 139.58
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 190
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 53566-95-3
Molecular Formula: C20H15NO2
Molecular Weight: 301.35
Purity/Analysis Method: >95.0% (GC)
Form: Crystal
Melting point (°C): 142
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 434-75-3
MDL Number: MFCD00002417
Molecular Formula: C7H4ClFO2
Molecular Weight: 174.56
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 158
MSDS SDS
Catalog Number: (TCS0449-025G)

Supplier:  TCI America
Description:   CAS Number: 2050-23-9
MDL Number: MFCD00009217
Molecular Formula: C12H22O4
Molecular Weight: 230.30
Purity/Analysis Method: >98.0% (GC)
Form: Clear Liquid
Color: Colorless
Boiling point (°C): 283
Flash Point (°C): 110
Specific Gravity (20/20): 0.98
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 1137-41-3
MDL Number: MFCD00007895
Molecular Formula: C13H11NO
Molecular Weight: 197.24
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 123
MSDS SDS
Catalog Number: (77439-428)

Supplier:  Bioss
Description:   The FOX family of transcription factors share a common DIUA binding domain termed a winged-helix or forkhead domain. Many FOX proteins play important roles in development, metabolism, cancer and aging. FOXD1 (also designated Brain Factor 2 or BF-2) is involved in regulating inflammation as well as kidney and retinal development. FOXD1 regulates the activity of NF-AT and NFkB. Deficiency of FOXD1 results in multiorgan, systemic inflammation, exaggerated Th cell-derived cytokine production, and T cell proliferation in autogolgous MLRs. In kidneys, FOXD1 controls the production of signals required for the normal transition of induced mesenchyme into tubular epithelium and full growth and branching of the collecting system. Deletion of FOXD1 results in renal abnormalities. FOXD2 acts as a modulator of T cell activation.
Supplier:  TCI America
Description:   [for Molten Salt]
CAS Number: 155371-19-0
MDL Number: MFCD00216703
Molecular Formula: C6H11F6N2P
Molecular Weight: 256.13
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 61
MSDS SDS

Supplier:  INSTECH LABORATORIES, INC
Description:   The Pump 11 Elite series expands the capabilities of the original workhorse Pump 11 series with a high resolution touchscreen and intuitive icon interface. The interface allows users to create, save, and run simple to complex methods without a PC.
New Product
Supplier:  TCI America
Description:   CAS Number: 50-45-3
Molecular Formula: C7H4Cl2O2
Molecular Weight: 191.01
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 169
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 24241-18-7
Molecular Formula: C4H3Br2N3
Molecular Weight: 252.90
Purity/Analysis Method: >98.0% (GC)
Form: Crystal
Melting point (°C): 114
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 128-97-2
Molecular Formula: C14H8O8
Molecular Weight: 304.21
Purity/Analysis Method: >60.0% (NMR)
Form: Crystal
Storage Temperature: 0-10°C
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 26576-85-2
MDL Number: MFCD01632121
Molecular Formula: C10H16BrN
Molecular Weight: 230.15
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
MSDS SDS
Supplier:  TCI America
Description:   CAS Number: 3096-71-7
Molecular Formula: C8H11NO
Molecular Weight: 137.18
Purity/Analysis Method: >97.0% (GC,T)
Form: Crystal
Melting point (°C): 238
MSDS SDS
Catalog Number: (10100-306)

Supplier:  Prosci
Description:   This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mouse studies suggest that LPIN1 functions during normal adipose tissue development and may also play a role in human triglyceride metabolism. This gene represents a candidate gene for human lipodystrophy, characterized by loss of body fat, fatty liver, hypertriglyceridemia, and insulin resistance. Mouse studies suggest that this gene functions during normal adipose tissue development and may also play a role in human triglyceride metabolism. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Catalog Number: (10107-214)

Supplier:  Prosci
Description:   DLX5 is a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. This protein may play a role in bone development and fracture healing. Mutation in its gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation.
Catalog Number: (10107-288)

Supplier:  Prosci
Description:   SOX3 is a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked mental retardation with growth hormone deficiency.This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. Mutations in this gene have been associated with X-linked mental retardation with growth hormone deficiency.
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