You Searched For: D-Glucono-1,5-lactone


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Supplier: Abcam
Description: Rabbit monoclonal [EPR22506-15] to Rad21 - ChIP Grade.

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Catalog Number: (10061-736)
Supplier: Prosci
Description: 15 amino acids near the amino terminus of human STAT3.


Supplier: Ace Glass
Description: Chemically inert PTFE adapters feature either a #15 or #25 Ace-Thred.

Small Business Enterprise Product available on GSA Advantage®

Catalog Number: (ABCA_AB28118-100UG)
Supplier: Abcam
Description: Biotin Mouse monoclonal [MEM-15] to CD14.

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Catalog Number: (77179-978)
Supplier: ANTIBODIES.COM LLC
Description: Mouse monoclonal [IL15/4696] antibody to IL-15 for IHC-P with samples derived from Human.


Catalog Number: (77182-928)
Supplier: ANTIBODIES.COM LLC
Description: Recombinant Human IL-15RA + IL-15 (from HEK293 cells)


Catalog Number: (103886-848)
Supplier: Sino Biological
Description: A DNA sequence encoding the influenza A virus (A/swine/Iowa/15/1930 (H1N1)) neuraminidase (AAF77044) (His36-Lys469), termed as NA, was fused with a N-terminal polyhistidine tag.


Supplier: AFG Bioscience
Description: 2-​Acetamidoglucal 95%

Supplier: GRANT USA INC.
Description: For 12 x 15 ml tubes with caps and conical bottom

Catalog Number: (10492-272)
Supplier: Bioss
Description: RPUSD2, is a 545 amino acid member of the pseudouridine synthase rluA family and is encoded by a gene that is located on chromosome 15. Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this region from the paternal copy of chromosome 15. Tay-Sachs disease is a lethal disorder associated with mutations of the HEXA gene, which is encoded by chromosome 15. Marfan syndrome is associated with chromosome 15 through the FBN1 gene.


Supplier: SUPERTEK SCIENTIFIC LLC
Description: Explore the Kingdom Protista.

Supplier: Abcam
Description: Rabbit monoclonal [EPR26286-15] to Nogo A + Nogo D.

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Supplier: Abcam
Description: Rabbit monoclonal [EPR16805-15] to IL-1 beta.

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Supplier: Abcam
Description: Rabbit monoclonal [EPR26993-15] to Plectin - BSA and Azide free (Detector).

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Catalog Number: (TCB3339-25G)
Supplier: TCI America
Description: CAS Number: 52490-15-0
MDL Number: MFCD00040947
Molecular Formula: C19H18O3
Molecular Weight: 294.35
Purity/Analysis Method: >98.0% (GC,T)
Form: Crystal
Melting point (°C): 119

Supplier: Abcam
Description: APC Rabbit monoclonal [EPR22354-15] to CX3CR1.

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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.
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