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4-Bromo-2-fluorophenyl+isothiocyanate


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Catalog Number: (76457-446)

Supplier:  VWR International
Description:   VWR® Stainless Steel Surgical Scalpel Blades are made from sharp, long lasting surgical stainless steel.
Supplier:  VWR International
Description:   Standing height steel storage cabinets are 84" high and 12<sup>3</sup>/<sub>4</sub>", 16", or 22" deep.
Product available on GSA Advantage®
Supplier:  Rockland Immunochemical
Description:   FGF13(Fibroblast growth factor 13), also called FHF2 is a protein that in humans is encoded by the FGF13 gene.The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF13is a large gene, extending over approximately 200 kb in Xq26.3, and contains at least 7 exons. By cytogenetic, FISH, and database analysis, Gecz et al. (1999) localized the FGF13 gene within a 400-kb duplication interval on chromosome Xq26.3. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. Other areas of interests and use for researchers include cancer, borjeson-forssman-lehmann syndrome, regulation of actin cytoskeleton pathways, apoptosis, GPCR pathways, TGF-Beta pathways, and Rho familty GTPase pathways. This gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.

Supplier:  Rockland Immunochemical
Description:   FGF13(Fibroblast growth factor 13), also called FHF2 is a protein that in humans is encoded by the FGF13 gene.The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF13is a large gene, extending over approximately 200 kb in Xq26.3, and contains at least 7 exons. By cytogenetic, FISH, and database analysis, Gecz et al. (1999) localized the FGF13 gene within a 400-kb duplication interval on chromosome Xq26.3. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. Other areas of interests and use for researchers include cancer, borjeson-forssman-lehmann syndrome, regulation of actin cytoskeleton pathways, apoptosis, GPCR pathways, TGF-Beta pathways, and Rho familty GTPase pathways. This gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.
Supplier:  AMBEED, INC
Description:   Sodium 3-oxo-3H-benzo[d]isothiazol-2-ide 1,1-dioxide xhydrate, Purity: 97%, CAS Number: 82385-42-0, Appearance: Colorless or White Powder or Crystals, Storage: Inert atmosphere, Room Temperature, Size: 500G
Catalog Number: (76008-992)

Supplier:  Prosci
Description:   This gene is one of several cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. This protein is similar to CCL4 which inhibits HIV entry by binding to the cellular receptor CCR5. The copy number of this gene varies among individuals; most individuals have 1-5 copies in the diploid genome, although rare individuals do not contain this gene at all. The human genome reference assembly contains two copies of this gene. This record represents the more centromeric gene. [provided by RefSeq].
Supplier:  VWR International
Description:   For twenty-four 22-25mm test tubes. An accessory for VWR* Mini and Incubating Mini Shakers and for VWR Incubating Shakers.
Product available on GSA Advantage®
Supplier:  Rockland Immunochemical
Description:   FGF13(Fibroblast growth factor 13), also called FHF2 is a protein that in humans is encoded by the FGF13 gene.The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF13is a large gene, extending over approximately 200 kb in Xq26.3, and contains at least 7 exons. By cytogenetic, FISH, and database analysis, Gecz et al. (1999) localized the FGF13 gene within a 400-kb duplication interval on chromosome Xq26.3. FGF family members possess broad mitogenic and cell survival activities, and are involved in a variety of biological processes, including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. Other areas of interests and use for researchers include cancer, borjeson-forssman-lehmann syndrome, regulation of actin cytoskeleton pathways, apoptosis, GPCR pathways, TGF-Beta pathways, and Rho familty GTPase pathways. This gene is located to a region associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a syndromal X-linked mental retardation, which suggests it may be a candidate gene for familial cases of the BFL syndrome. The function of this gene has not yet been determined. Two alternatively spliced transcripts encoding different isoforms have been described for this gene.
Supplier:  TCI America
Description:   CAS Number: 6381-59-5
MDL Number: MFCD00150989
Molecular Formula: C4H6O6
Molecular Weight: 210.16
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Color: White
Melting point (°C): 80
Specific rotation [a]20/D: 22 deg (C=10, H2O)
Catalog Number: (10800-632)

Supplier:  Rockland Immunochemical
Description:   CCDC22 is a recently identified coiled-coil domain-containing protein that has been shown to bind copines, which are calcium-dependent, membrane-binding proteins that may function in calcium signaling. In rat, CCDC22 has been observed to localize in multiple regions of the brain, including the prefrontal and somatosensory cortex, dentate gyrus and thalamus, and in the ipsilateral motor neurons of the spinal cord after sciatic nerve transection suggesting that it may play a role in neuronal injury response. The human CCDC22 gene has been identified as a novel candidate gene for syndromic X-linked intellectual disability (XLID).

Supplier:  AOB CHEM USA
Description:   4-Bromo-3-chloro-2,4'-difluoro-1,1'-biphenyl ≥97%

Supplier:  VWR International
Description:   VWR® Sterile Disposable Scalpels are mounted on plastic handles with fluted finger-grips.
Supplier:  VWR International
Description:   Suitable for organic synthesis, cleaning, and prep scale synthesis. Contains ~1ppm BHT as preservative.
MSDS SDS
Supplier:  VWR International
Description:   BDH* Ethyl Ether Anhydrous, Chemical Formula: (C2H5)2O, Melting Point: -116.3, Boiling Point: 34.5, Flash Point: -45 deg C, Formula Weight: 74.12, CAS Number: 60-29-7, Grade: HPLC/Spectro, HiPerSolv CHROMANORM, Class: F, Size: 4L
MSDS SDS
Supplier:  Promega Corporation
Description:   A fast, simple technique for preparation of intact total RNA from tissues, cultured cells and white blood cells in as little as one hour.
MSDS SDS
Supplier:  Promega Corporation
Description:   The MethylEdge Bisulfite Conversion System provides a rapid, efficient method to perform bisulfite conversion with minimal DNA fragmentation in less than two hours.
MSDS SDS
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
449 - 464  of 141,884
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