Text Search >
Ace+Method+Development+Kits
Print…
You Searched For:
97,317 results were found
Ace+Method+Development+Kits
Supplier:
Yamato Scientific
Description:
The air-jacket technology of these incubators ensures even and efficient heat distribution throughout the chamber.
Catalog Number:
(TCT0147-100ML)
Supplier:
TCI America
Description:
CAS Number: 110-18-9
MDL Number: MFCD00008335
Molecular Formula: C6H16N2
Molecular Weight: 116.21
Purity/Analysis Method: <gt/>98.0% (GC,T)
Form: Clear Liquid
Color: Colorless
Boiling point (°C): 122
Melting point (°C): -55
Flash Point (°C): 17
Specific Gravity (20/20): 0.78
Catalog Number:
(TCT2309-25G)
Supplier:
TCI America
Description:
CAS Number: 59-02-9
Molecular Formula: C29H50O2 Molecular Weight: 430.72 Purity/Analysis Method: >97.0% (GC) Form: Clear Liquid Color: Pale Yellow Melting point (°C): 4 Flash Point (°C): 253 Specific Gravity (20/20): 0.95 Specific rotation [a]20/D: 0.5 deg (C=1, EtOH)
Catalog Number:
(10480-572)
Supplier:
Bioss
Description:
DHRSX (dehydrogenase/reductase SDR family member on chromosome X) is a 330 amino acid protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, DHRSX is an oxidoreductase that contains a coenzyme binding site and a substrate binding site, indicating a possible role in cellular metabolism. The gene that encodes DHRSX is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Catalog Number:
(10480-582)
Supplier:
Bioss
Description:
DHRSX (dehydrogenase/reductase SDR family member on chromosome X) is a 330 amino acid protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, DHRSX is an oxidoreductase that contains a coenzyme binding site and a substrate binding site, indicating a possible role in cellular metabolism. The gene that encodes DHRSX is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Catalog Number:
(10480-576)
Supplier:
Bioss
Description:
DHRSX (dehydrogenase/reductase SDR family member on chromosome X) is a 330 amino acid protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, DHRSX is an oxidoreductase that contains a coenzyme binding site and a substrate binding site, indicating a possible role in cellular metabolism. The gene that encodes DHRSX is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
Catalog Number:
(TCS0835-100MG)
Supplier:
TCI America
Description:
CAS Number: 152-95-4
MDL Number: MFCD01075138 Molecular Formula: C21H20O10 Molecular Weight: 432.38 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Color: Pale Yellow Melting point (°C): 297 Specific rotation [a]20/D: -18 deg (C=1, Pyridine) Lambda max.: 271 nm (MeOH)
Catalog Number:
(76101-522)
Supplier:
Bioss
Description:
Transcriptional corepressor which does not bind directly to DNA and may regulate transcription through recruitment of histone deacetylases to gene promoters. Regulates cell adhesion, migration and proliferation. May be required for segmental gene expression during hindbrain development.
Catalog Number:
(10107-542)
Supplier:
Prosci
Description:
GRHL3 is a member of the grainyhead family of transcription factors. GRHL3 interacts with leader-binding protein 32 (LBP-32) and brother of mammalian grainyhead (BOM), and may function as a transcription factor during development. Multiple transcript variants encoding distinct isoforms have been identified for this gene. This gene encodes a member of the grainyhead family of transcription factors. The encoded protein interacts with leader-binding protein 32 (LBP-32) and brother of mammalian grainyhead (BOM), and may function as a transcription factor during development. Multiple transcript variants encoding distinct isoforms have been identified for this gene. Additional transcript variants have been described, but their biological nature has not been determined.
Catalog Number:
(89360-598)
Supplier:
Genetex
Description:
The c-Myc protein is a transcription factor, which is encoded by the c-Myc gene on human chromosome 8q24. c-Myc is commonly activated in a variety of tumor cells and plays an important role in cellular proliferation, differentiation, apoptosis and cell cycle progression. The phosphorylation of c-Myc has been investigated and previous studies have suggested a functional association between phosphorylation at Thr58/Ser62 by glycogen synthase kinase 3, cyclin-dependent kinase, ERK2 and C-Jun N-terminal Kinase (JNK) in cell proliferation and cell cycle regulation. Studies also have shown that c-Myc is essential for tumor cell development in vasculogenesis and angiogenesis that distribute blood throughout the cells, and which brought extensive attention in the development of new therapeutic approach for cancer treatment.
Catalog Number:
(10110-204)
Supplier:
Prosci
Description:
The function remains unknown.
Catalog Number:
(10108-648)
Supplier:
Prosci
Description:
The function remains unknown.
Catalog Number:
(10102-900)
Supplier:
Prosci
Description:
The function remains unknown.
Catalog Number:
(TCB1219-100MG)
Supplier:
TCI America
Description:
[for Optical Resolution]
CAS Number: 87248-50-8 MDL Number: MFCD00074783 Molecular Formula: C24H38O3 Molecular Weight: 374.57 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Melting point (°C): 151 Specific rotation [a]20/D: 202.5 deg (C=2, THF)
Catalog Number:
(75793-036)
Supplier:
Prosci
Description:
Three receptors for BAFF were recently identified and designated TACI, BCMA and BAFF-R. BAFF-R signaling is essential for B cell development, survival and humoral immune responses.
Supplier:
TCI America
Description:
CAS Number: 14804-38-7
MDL Number: MFCD00143259 Molecular Formula: C9H11BrO Molecular Weight: 215.09 Purity/Analysis Method: >96.0% (GC) Form: Clear Liquid Boiling point (°C): 120 Flash Point (°C): 110 Specific Gravity (20/20): 1.36
Inquire for Price
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
 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
is still displayed and you need assistance, please call us at 1-800-932-5000.
You must log in to order restricted items. We request that you provide the required business documentation to purchase this product for the first time.
To order chemicals, medical devices, or other restricted products please provide identification that includes your business name and shipping address via email CMD_NA@vwr.com or fax 484.881.5997 referencing your VWR account number . Acceptable forms of identification are:
-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 currently unavailable but limited stock may be available in our extended warehouse network. Please call 1-800-932-5000 and a VWR Customer Service Representative will help you.
|
|||||||||
List View
