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Catalog Number:
(10491-372)
Supplier:
Bioss
Description:
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 an 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 unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as 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. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.
Catalog Number:
(10495-666)
Supplier:
Bioss
Description:
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 an 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 unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as 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. The CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.
Catalog Number:
(10491-354)
Supplier:
Bioss
Description:
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 an 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 unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as 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. The CXX1 gene product has been provisionally designated CXX1 pending further characterization.
Catalog Number:
(76108-382)
Supplier:
Bioss
Description:
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 an 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 unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as 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. The FAM104B gene product has been provisionally designated FAM104B pending further characterization.
Supplier:
Environmental Express
Description:
The FlipMate™ system easily filters the sample with the use of two threaded digestion cups, a filter assembly, vacuum tubing, and vacuum pressure source.
Supplier:
Shenandoah Biotechnology
Description:
Nerve growth factor beta (β-NGF) is a neurotrophic factor that is important for the development and maintenance of sensory and sympathetic neurons. β-NGF signals through the low affinity nerve growth factor receptor (LNGFR) and the tropomyosin receptor kinase A (TrkA) to activate PI3K, Ras, and PLC signaling pathways. β-NGF is also involved in the growth, differentiation, and survival of B lymphocytes. Human, mouse, and rat β-NGF proteins are cross-reactive.
Catalog Number:
(77439-124)
Supplier:
Bioss
Description:
Transcription factor that seems to function synergistically with the POU domain protein TST-1/OCT6/SCIP. Could confer cell specificity to the function of other transcription factors in developing and mature glia (By similarity).
Catalog Number:
(10101-732)
Supplier:
Prosci
Description:
OTP is probably involved in the differentiation of hypothalamic neuroendocrine cells.This gene encodes a member of the homeodomain (HD) family. HD family proteins are helix-turn-helix transcription factors that play key roles in the specification of cell fates. This protein may function during brain development.
Catalog Number:
(89361-424)
Supplier:
Genetex
Description:
The NUMB and Numb-like genes are essential during nervous system development. Numb proteins function to maintain the self-renewal properties of all neural progenitor cells and could play similar roles in stem-cell maintenance in other tissues. Mice ablated for either NUMB or Numb-like in the nervous system are born normally, however deletion of both genes results in embryonic lethality (E11.5).
Catalog Number:
(10092-368)
Supplier:
Proteintech
Description:
PITX1, also named as Pituitary homeobox 1 or BFT, is a 314 amino acid protein, which contains one homeobox DNA-binding domain and belongs to the paired homeobox family. Bicoid subfamily. PITX1 localizes in the nucleus and may play a role in the development of anterior structures, and in particular, the brain and facies and in specifying the identity or structure of hindlimb.
Catalog Number:
(10085-436)
Supplier:
Proteintech
Description:
CXCR7 (C-X-C chemokine receptor type 7), also known as RDC1, is a member of the G-protein coupled receptor family. CXCR7 can bind the chemokines CXCL11 and CXCL12 with high affinity, and it also acts as coreceptor with CXCR4 for a restricted number of HIV isolates. Expression of CXCR7 has been associated with cardiac development as well as with tumor growth and progression.
Supplier:
TCI America
Description:
CAS Number: 1193-62-0
MDL Number: MFCD00817048 Molecular Formula: C6H7NO2 Molecular Weight: 125.13 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 73
Catalog Number:
(470315-958)
Supplier:
Fabrication Enterprises
Description:
The Skyndex® digital skinfold caliper was developed to use with the general population and is a fast way to assess the body fat level of groups of people using body fat calipers.
Supplier:
TCI America
Description:
CAS Number: 5222-73-1
MDL Number: MFCD00101316 Molecular Formula: C6H6O4 Molecular Weight: 142.11 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 56
Catalog Number:
(TCC0974-025G)
Supplier:
TCI America
Description:
CAS Number: 3752-25-8
MDL Number: MFCD00004372 Molecular Formula: C9H7ClO2 Molecular Weight: 182.60 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Melting point (°C): 210
Supplier:
TCI America
Description:
CAS Number: 65427-54-5
MDL Number: MFCD00012910 Molecular Formula: C4H10N2O2 Molecular Weight: 191.05 Purity/Analysis Method: >98.0% (N,T) Form: Crystal Melting point (°C): 203
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