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Product Image-76654-162

Cyclobutylboronic acid MIDA ester 97%

Supplier: Ambeed
Description: 8-Cyclobutyl-4-methyl-2,6-dioxohexahydro-[1,3,2]oxazaborolo[2,3-b][1,3,2]oxazaborol-4-ium-8-uide, Purity: 97%, CAS Number: 1104637-37-7, Appearance: Form: solid, Storage: Inert atmosphere, Room Temperature, Size: 1G

Image Unavailable-77141-204

4-Pyridinylboronic acid MIDA ester 97%

Catalog Number: (77141-204)
Supplier: Ambeed
Description: 4-Pyridinylboronic acid MIDA ester, Purity: 97%, CAS Number: 1104636-72-7, Appearance: Solid, Storage: Sealed in dry, 2-8 deg C, Size: 5g
Image Unavailable-77622-732

5-Bromo-2-thiophenylboronic acid mida ester ≥95%

Catalog Number: (77622-732)
Supplier: Ambeed
Description: 5-Bromo-2-thiophenylboronic acid mida ester ≥95%

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Image Unavailable-76823-754

Cyclopropylboronic acid MIDA ester 97%

Supplier: Ambeed
Description: Cyclopropylboronic acid MIDA ester, Purity: 97%, CAS Number: 1104637-36-6, Appearance: White to beige Powder or Crystals, Storage: Sealed in dry, 2-8C, Size: 250MG

Image Unavailable-77118-576

3-Bromophenylboronic acid MIDA ester 95%

Supplier: Ambeed
Description: 3-Bromophenylboronic acid MIDA ester, Purity: 95%, CAS Number: 943552-25-8, Appearance: White to beige Powder or Crystals, Storage: Sealed in dry, Room Temperature, Size: 1g

Product Image-76654-462

2-(4-Hydroxyphenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione 95+%

Supplier: Ambeed
Description: 4-Hydroxyphenylboronic acid MIDA ester, Purity: 95+%, CAS Number: 1613586-40-5, Appearance: Solid, Storage: Inert atmosphere, Room Temperature, Size: 100G

Product Image-76667-976

(3-((2-(Diethylamino)ethyl)carbamoyl)phenyl)boronic acid MIDA ester 98%

Supplier: Ambeed
Description: (3-((2-(Diethylamino)ethyl)carbamoyl)phenyl)boronic acid MIDA ester, Purity: 98%, CAS Number: 2828439-48-9, Appearance: Solid, Storage: Sealed in dry, 2-8C, Size: 1G

Product Image-76673-748

4-(6-Methyl-4,8-dioxo-1,3,6,2-dioxazaborocan-2-yl)benzaldehyde 95%

Catalog Number: (76673-748)
Supplier: Ambeed
Description: 4-Formylphenylboronic acid MIDA ester, Purity: 95%, CAS Number: 1072960-66-7, Appearance: Solid, Storage: Inert atmosphere, Room Temperature, Size: 250MG
Product Image-76673-740

2-(4-Iodophenyl)-6-methyl-1,3,6,2-dioxazaborocane-4,8-dione 98%

Supplier: Ambeed
Description: 4-Iodophenylboronic acid MIDA ester, Purity: 98%, CAS Number: 1287221-36-6, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 5G

Image Unavailable-77311-602

Cyclobutylboronic acid 97%

Catalog Number: (77311-602)
Supplier: Ambeed
Description: Cyclobutylboronic acid 97%
Image Unavailable-10316-470

Anti-C2orf56 Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (10316-470)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Image Unavailable-10316-468

Anti-C2orf56 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (10316-468)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Image Unavailable-76098-918

Anti-C2orf56 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (76098-918)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Image Unavailable-10311-402

Anti-C2orf56 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (10311-402)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Image Unavailable-10311-404

Anti-C2orf56 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Catalog Number: (10311-404)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
Image Unavailable-10311-400

Anti-C2orf56 Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (10311-400)
Supplier: Bioss
Description: C12orf56 (chromosome 12 open reading frame 56), also known as PRO1853 or protein midA homolog, is a 441 amino acid mitochondrial protein that belongs to the midA family. Existing as two alternatively spliced isoforms, C12orf56 is encoded by a gene that maps to human chromosome 2p22.2. As the second largest human chromosome, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is related to mutations in the ALMS1 gene. Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, which are still present in modern day apes.
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