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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-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-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
Image Unavailable-BOSSBS-13282R-CY3

Anti-GAPDHS Rabbit Polyclonal Antibody (Cy3®)

Beskrivelse: May play an important role in regulating the switch between different pathways for energy production during spermiogenesis and in the spermatozoon. Required for sperm motility and male fertility (By similarity).
Varenummer: BOSSBS-13282R-CY3
UOM: 1 * 100 µl
Leverandør: Bioss
Product Image-MFLX30401-38

Masterflex® Plug Fittings, Male NPT Threaded, Straight, Avantor®

Beskrivelse: Deigned for permanent connection.
Varenummer: MFLX30401-38
UOM: 1 * 10 Items
Leverandør: Avantor Fluid Handling
Product Image-BOHLF763-08

Connectors, screw-in tube fittings, BOLA

Beskrivelse: Straight UNF screw-in tube fitting made of PTFE. One side with fitting thread GL 14 for connecting hard-walled tubes and tubing by means of BOLA Laboratory Screw Joints. Other side with male screw-in thread UNF 1/4 28G for connection to units and fittings with female thread UNF 1/4 28G.
Varenummer: BOHLF763-08
UOM: 1 * 1 Items
Leverandør: Bohlender
Image Unavailable-BOSSBS-8263R-A488

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

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-A488
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-8263R-HRP

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

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-HRP
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-8480R-CY7

Anti-RBMX2 Rabbit Polyclonal Antibody (Cy7®)

Beskrivelse: RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. 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. 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 that affect males more frequently as males carry a single X chromosome.
Varenummer: BOSSBS-8480R-CY7
UOM: 1 * 100 µl
Leverandør: Bioss
Image Unavailable-BOSSBS-8480R-CY5

Anti-RBMX2 Rabbit Polyclonal Antibody (Cy5®)

Beskrivelse: RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. 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. 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 that affect males more frequently as males carry a single X chromosome.
Varenummer: BOSSBS-8480R-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
Image Unavailable-MILLZLXL00ESVSD

Accessories for Water Purification Systems, Milli-Q® HX 7040/7080/7120/7150 SD

Beskrivelse: External magnetic valve for Milli-Q® HX SD with ³/₄" male thread, Til: Water purification systems, Milli-Q® HX 7040/7080/7120/7150 SD
Varenummer: MILLZLXL00ESVSD
UOM: 1 * 1 Items
Leverandør: Merck

New Product


Image Unavailable-BOSSBS-8480R-A680

Anti-RBMX2 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Beskrivelse: RBMX2 is a 322 amino acid member of the IST3 family that contains one RRM (RNA recognition motif) domain. The RBMX2 gene is intronless, conserved in chimpanzee, dog, cow, mouse, rat, zebrafish, fruit fly, mosquito, C.elegans, S.pombe, S.cerevisiae, K.lactis, E.gossypii, M.grisea, N.crassa, A.thaliana, rice and P.falciparum, and maps to human chromosome Xq25. 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. 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 that affect males more frequently as males carry a single X chromosome.
Varenummer: BOSSBS-8480R-A680
UOM: 1 * 100 µl
Leverandør: Bioss
Product Image-MFLX15973-45BLK

Value Plastics Luer Fittings and Adapters

Beskrivelse: Premium luer fittings for critical applications.
Varenummer: MFLX15973-45BLK
UOM: 1 * 1.000 Items
Leverandør: Avantor Fluid Handling

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