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Methyl cholate 98+%

Supplier: Thermo Scientific Chemicals
Description: Methyl cholate 98+%

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Image Unavailable-103007-372

Histone H4 (1-21) Substrate

Catalog Number: (103007-372)
Supplier: Anaspec Inc
Description: This sequence is amino acids 1 to 21 fragment of the histone 4. Histone acetyltransferase (HAT) p300/CBP catalyses the acetylation of this N-terminal tail of free histone H4 at Lys5, 8, 12, 16. Lys8 is thought to be the preferred acetylation site in H4. Determinants of interaction of p300 with histone 4 appear to be fully present on H4-21, the N-terminal region of the protein.
Sequence:SGRGKGGKGLGKGGAKRHRKV
MW:2091.5 Da
% peak area by HPLC:95
Storage condition:-20° C
Image Unavailable-76109-032

Anti-GLT8D2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76109-032)
Supplier: Bioss
Description: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
Image Unavailable-10481-456

Anti-GLT8D2 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10481-456)
Supplier: Bioss
Description: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
Image Unavailable-10481-276

Anti-GLT8D2 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10481-276)
Supplier: Bioss
Description: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
Image Unavailable-76109-030

Anti-GLT8D2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76109-030)
Supplier: Bioss
Description: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
Image Unavailable-10477-524

Anti-CCDC38 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (10477-524)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Product Image-RC270025

EDTA disodium salt 0.0100 M (M/100) in aqueous solution

Supplier: Ricca Chemical
Description: EDTA disodium salt 0.0100 M (M/100) in aqueous solution analytical reagent

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Image Unavailable-TCI0214-025G

Indigo carmine ≥95.0% (by UV method)

Catalog Number: (TCI0214-025G)
Supplier: TCI America
Description: CAS Number: 860-22-0
MDL Number: MFCD00005723
Molecular Formula: C16H10N2O8S2
Molecular Weight: 466.35
Purity/Analysis Method: >95.0% (E)
Form: Crystal

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Product Image-RC2705-16

EDTA disodium salt 0.0500 M (M/20) in aqueous solution ASTM D 2036 D titrant

Catalog Number: (RC2705-16)
Supplier: Ricca Chemical

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Image Unavailable-10477-186

Anti-CCDC38 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10477-186)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Image Unavailable-76107-226

Anti-CCDC38 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76107-226)
Supplier: Bioss
Description: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Image Unavailable-CAAAH33334-06

Methyl-2-hydroxynicotinate 97%

Supplier: Thermo Scientific Chemicals

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Product Image-10085-516

Anti-CYP2C8 Rabbit Polyclonal Antibody

Catalog Number: (10085-516)
Supplier: Proteintech
Description: CYP2C8(Cytochrome P450 2C8) is also named as CYPIIC8, cytochrome P450 IIC2, cytochrome P450 MP-12, cytochrome P450 MP-20, cytochrome P450 form 1 and S-mephenytoin 4-hydroxylase. It belongs to the cytochrome P450 family. It is a monooxygenase involved in an NADPH-dependent electron transport pathway and a hepatic drug-metabolizing enzymes that oxidizes therapeutic drugs such as taxol and cerivastatin and endobiotics such as retinoic acid and arachidonic acid. It has 2 isoforms produced by alternative splicing.
Image Unavailable-76085-370

Anti-SLC27A2/ACSVL1 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (76085-370)
Supplier: Bioss
Description: Acyl-CoA synthetase probably involved in bile acid metabolism. Proposed to activate C27 precurors of bile acids to their CoA thioesters derivatives before side chain cleavage via peroxisomal beta-oxidation occurs. In vitro, activates 3-alpha,7-alpha,12-alpha-trihydroxy-5-beta-cholestanate (THCA), the C27 precursor of cholic acid deriving from the de novo synthesis from cholesterol. Does not utilize C24 bile acids as substrates. In vitro, also activates long- and branched-chain fatty acids and may have additional roles in fatty acid metabolism. May be involved in translocation of long-chain fatty acids (LFCA) across membranes (By similarity).
Image Unavailable-75812-154

Sodium L(+)-ascorbate ≥99.0% FCC

Supplier: Spectrum Chemicals
Description: Sodium Ascorbate, FCC is used as a food additive as an antioxidant and acidity regulator. The FCC grade meets the requirements of the Food Chemical Codex indicates and is suitable for all food, beverage and nutritional supplement applications. Spectrum Chemical offers over 300 Food grade chemical ingredients packaged in laboratory size bottles to production drum quantities and are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities

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