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Image Unavailable-BOSSBS-13610R-A680

Anti-HCG3 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Beskrivelse: May operate as a co-chaperone of the male germ cell- and haploid stage-specific Hsp70 proteins.
Varenummer: BOSSBS-13610R-A680
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-8263R-A555

Anti-DHRSX Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Beskrivelse: 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.
Varenummer: BOSSBS-8263R-A555
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-11006R-CY3

Anti-TMEM255A Rabbit Polyclonal Antibody (Cy3®)

Beskrivelse: 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 FAM70A gene product has been provisionally designated FAM70A pending further characterization.
Varenummer: BOSSBS-11006R-CY3
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9552R-CY3

Anti-CXORF21 Rabbit Polyclonal Antibody (Cy3®)

Beskrivelse: 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 CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.
Varenummer: BOSSBS-9552R-CY3
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-11397R-CY7

Anti-ARG2 Rabbit Polyclonal Antibody (Cy7®)

Beskrivelse: May play a role in the regulation of extra-urea cycle arginine metabolism and also in down-regulation of nitric oxide synthesis. Extrahepatic arginase functions to regulate L-arginine bioavailability to NO synthase. Since NO synthase is found in the penile corpus cavernosum smooth muscle, the clitoral corpus cavernosum and the vagina, arginase II plays a role in both male and female sexual arousal. It is therefore a potential target for the treatment of male and female sexual arousal disorders.
Varenummer: BOSSBS-11397R-CY7
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9553R-CY5.5

Anti-FAM127A Rabbit Polyclonal Antibody (Cy5.5®)

Beskrivelse: 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.
Varenummer: BOSSBS-9553R-CY5.5
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9553R-CY3

Anti-FAM127A Rabbit Polyclonal Antibody (Cy3®)

Beskrivelse: 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.
Varenummer: BOSSBS-9553R-CY3
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-11006R-FITC

Anti-TMEM255A Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Beskrivelse: 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 FAM70A gene product has been provisionally designated FAM70A pending further characterization.
Varenummer: BOSSBS-11006R-FITC
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9550R-A488

Anti-CXORF56 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Beskrivelse: 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.
Varenummer: BOSSBS-9550R-A488
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9550R-A555

Anti-CXORF56 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Beskrivelse: 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.
Varenummer: BOSSBS-9550R-A555
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9551R-A750

Anti-BEND2 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Beskrivelse: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates proteinDNA and proteinprotein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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.
Varenummer: BOSSBS-9551R-A750
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-11276R-A350

Anti-DMRT1 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Beskrivelse: Transcription factor that plays a key role in male sex determination and differentiation by controlling testis development and male germ cell proliferation. Plays a central role in spermatogonia by inhibiting meiosis in undifferentiated spermatogonia and promoting mitosis, leading to spermatogonial development and allowing abundant and continuous production of sperm. Acts both as a transcription repressor and activator: prevents meiosis by restricting retinoic acid (RA)-dependent transcription and repressing STRA8 expression and promotes spermatogonial development by activating spermatogonial differentiation genes, such as SOHLH1. Also plays a key role in postnatal sex maintenance by maintaining testis determination and preventing feminization: represses transcription of female promoting genes such as FOXL2 and activates male-specific genes. May act as a tumor suppressor. May also play a minor role in oogenesis (By similarity).
Varenummer: BOSSBS-11276R-A350
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-11276R-A680

Anti-DMO/Dmrt1a Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Beskrivelse: Transcription factor that plays a key role in male sex determination and differentiation by controlling testis development and male germ cell proliferation. Plays a central role in spermatogonia by inhibiting meiosis in undifferentiated spermatogonia and promoting mitosis, leading to spermatogonial development and allowing abundant and continuous production of sperm. Acts both as a transcription repressor and activator: prevents meiosis by restricting retinoic acid (RA)-dependent transcription and repressing STRA8 expression and promotes spermatogonial development by activating spermatogonial differentiation genes, such as SOHLH1. Also plays a key role in postnatal sex maintenance by maintaining testis determination and preventing feminization: represses transcription of female promoting genes such as FOXL2 and activates male-specific genes. May act as a tumour suppressor. May also play a minor role in oogenesis (By similarity).
Varenummer: BOSSBS-11276R-A680
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-8231R-HRP

Anti-FAM104B Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Beskrivelse: 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.
Varenummer: BOSSBS-8231R-HRP
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-9551R-CY5

Anti-BEND2 Rabbit Polyclonal Antibody (Cy5®)

Beskrivelse: BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. 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.
Varenummer: BOSSBS-9551R-CY5
UOM: 1 * 100 µl
Leverandør: Bioss
Product Image-USBI038633

Anti-MSL1 Rabbit Polyclonal Antibody

Beskrivelse: Anti-MSL1 Rabbit Polyclonal Antibody
Varenummer: USBI038633
UOM: 1 * 200 µl
Leverandør: US Biological
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