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2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
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2-(4-Chlorophenyl)-2,2-difluoroacetic+acid
Catalog Number:
(77672-516)
Supplier:
AMBEED, INC
Description:
1-(4-Chlorophenyl)-4,4-dimethylpentan-3-one 97%
Supplier:
Matrix Scientific
Description:
2-{[(3-Chlorophenyl)amino]methyl}-1H-isoindole-1,3(2H)-dione
Catalog Number:
(TCC0976-5G)
Supplier:
TCI America
Description:
[Phosphorylating Agent]
CAS Number: 15074-54-1 MDL Number: MFCD00009704 Molecular Formula: C6H4Cl3O2P Molecular Weight: 245.42 Purity/Analysis Method: >97.0% (T) Form: Clear Liquid Boiling point (°C): 256 Flash Point (°C): 105 Specific Gravity (20/20): 1.52
Supplier:
AMBEED, INC
Description:
1-(4-Chlorophenyl)biguanide hydrochloride, Purity: 95%, CAS Number: 4022-81-5, Appearance: White to light-yellow solid, Storage: Inert atmosphere, Room Temperature, Size: 100mg
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 044130-1G , MDL Number: MFCD00794341
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 054704-1G , MDL Number: MFCD00052804
Catalog Number:
(76071-758)
Supplier:
Prosci
Description:
For WB starting dilution is: 1:1000
Catalog Number:
(75794-128)
Supplier:
Prosci
Description:
FGF-2 (Basic fibroblast growth factor) belongs to the FGF superfamily that is made up of 22 different fibroblast growth factor genes. FGF-2 and FGF-1 (acidic FGF) are unique in that they do not follow the conventional signal sequence for secretion. FGF-2 is found in five isoforms via alternative initiation of translation. Signaling of FGF-2 occurs through the high-affinity tyrosine kinase receptors FGFR1-4. FGF-2 is a potent wide-spectrum mitogen whose overexpression is associated with immortalization and unregulated cell proliferation in many tumors. FGF-2 functions in angiogenesis, cell survival, tissue repair, embryonic development and inflammation. FGF-2 is widely used to maintain the self-renewal of human embryonic stem cells (ESCs) and to induce pluripotent stem cells. FGF-2 is an established neurogenic factor for proliferation and differentiation of multipotent neural stem cells both during development and in the adult mouse brain as well.
Catalog Number:
(101849-426)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040395-500MG , MDL Number: MFCD12028223
Catalog Number:
(76099-496)
Supplier:
Bioss
Description:
C9orf169 (chromosome 9 open reading frame 169) is a 423 amino acid single-pass membrane protein that belongs to the clpA/clpB family and torsin subfamily. The gene encoding C9orf169 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(76099-538)
Supplier:
Bioss
Description:
C9orf5 (chromosome 9 open reading frame 5), also known as CG2, is a 911 amino acid multi-pass membrane protein that is widely expressed and exists as four alternatively spliced isoforms. The gene encoding C9orf5 maps to human chromosome 9, which consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Supplier:
AMBEED, INC
Description:
(11bR)-2,6-Bis(4-chlorophenyl)-4-hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide, Purity: 97%, CAS Number: 922711-71-5, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 100MG
Catalog Number:
(101786-362)
Supplier:
Matrix Scientific
Description:
MF=C7H4Clf3S MW=212.62 Cas=407-16-9 MDL=MFCD00040954 500Mg
Catalog Number:
(101930-750)
Supplier:
Matrix Scientific
Description:
MF=C14H9Cln2O2 MW=272.69 MDL=MFCD01859130 500Mg
Catalog Number:
(101850-154)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040775-500MG , MDL Number: MFCD01935956
Supplier:
TCI America
Description:
4-Chloro-N-methylbenzylamine, CAS Number: 104-11-0, Purity: 97.0%(GC), Molecular Formula: C8H10ClN, Molecular Weight: 155.63 g/mol, Physical Form: Solid, Size: 5G
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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
is still displayed and you need assistance, please call us at 1-800-932-5000.
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