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Ace+Method+Development+Kits
Catalog Number:
(75792-910)
Supplier:
Prosci
Description:
Three receptors for BAFF were recently identified and designated TACI, BCMA and BAFF-R. BAFF-R signaling is essential for B cell development, survival and humoral immune responses.
Supplier:
TCI America
Description:
CAS Number: 530-59-6
MDL Number: MFCD00004401 Molecular Formula: C11H12O5 Molecular Weight: 224.21 Purity/Analysis Method: >98.0% (GC,T) Form: Crystal Melting point (°C): 198
Catalog Number:
(89366-370)
Supplier:
Genetex
Description:
Rabbit Polyclonal Antibody to LEF1
Catalog Number:
(10480-576)
Supplier:
Bioss
Description:
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.
Catalog Number:
(10480-572)
Supplier:
Bioss
Description:
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.
Catalog Number:
(10480-582)
Supplier:
Bioss
Description:
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.
Catalog Number:
(10102-646)
Supplier:
Prosci
Description:
The exact function of C6orf134 remains unknown.
Catalog Number:
(10103-632)
Supplier:
Prosci
Description:
The specific function of MPPE1 is not yet known.
Catalog Number:
(10104-022)
Supplier:
Prosci
Description:
The specific function of TC2N is not yet known.
Catalog Number:
(10106-768)
Supplier:
Prosci
Description:
KCTD6 is a domain of potassium channel
Catalog Number:
(10104-354)
Supplier:
Prosci
Description:
The exact functions of FAM78A remain unknown.
Supplier:
TCI America
Description:
CAS Number: 86672-58-4
MDL Number: MFCD03272508 Molecular Formula: C16H14N2O2 Molecular Weight: 266.30 Purity/Analysis Method: >95.0% (HPLC) Form: Crystal Melting point (°C): 215 Storage Temperature: >-20°C
Supplier:
TCI America
Description:
CAS Number: 87-91-2
MDL Number: MFCD00009143 Molecular Formula: C8H14O6 Molecular Weight: 206.19 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Color: Colorless Boiling point (°C): 162 Flash Point (°C): 152 Specific Gravity (20/20): 1.21 Specific rotation [a]20/D: 7.8 deg (neat)
Catalog Number:
(TCB1220-100MG)
Supplier:
TCI America
Description:
[for Optical Resolution]
CAS Number: 108031-79-4 MDL Number: MFCD00151131 Molecular Formula: C24H38O3 Molecular Weight: 374.57 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Melting point (°C): 151 Specific rotation [a]20/D: -202.5 deg (C=2, THF)
Catalog Number:
(CAPI29130)
Supplier:
LIFE TECHNOLOGIES CORP CA
Description:
Biotinylated bovine serum albumin (B-BSA) is used as a positive control in biotin quantitation methods.
Catalog Number:
(TCD2549-001G)
Supplier:
TCI America
Description:
CAS Number: 23788-74-1
MDL Number: MFCD00063233 Molecular Formula: C13H18O5S Molecular Weight: 286.34 Purity/Analysis Method: >98.0% (GC) Form: Crystal Flash Point (°C): 110 Specific rotation [a]20/D: -8 deg (C=2, DMF) Storage Temperature: 0-10°C
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