ly-6c

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201061
  • EUR 342.00
  • EUR 230.00
  • 100 ug
  • 25 ug

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201062
  • EUR 439.00
  • EUR 272.00
  • 100 ug
  • 25 ug

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201063
  • EUR 342.00
  • EUR 230.00
  • 100 ug
  • 25 ug

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201064
  • EUR 300.00
  • EUR 258.00
  • 100 ug
  • 25 ug

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201065
  • EUR 384.00
  • EUR 258.00
  • 100 ug
  • 25 ug

Ly-6G / Ly-6C (Gr-1) Antibody

20-abx201066
  • EUR 425.00
  • EUR 272.00
  • 100 ug
  • 25 ug

Anti-Mouse Ly-6c antibody

STJ16100768 100 µg
EUR 604

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1A(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1A(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1B(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1B(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1CFB(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1CFB(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1F(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1F(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1F(V500) 500 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PE(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PE(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PP(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PP(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PP55(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PP55(V25) 25 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PU(V100) 100 ug
EUR 50

Mouse Anti-Ly-6G/Ly-6C (Gr-1)

MOGR-1PU(V500) 500 ug
EUR 50

Sarafotoxin 6c

5-01901 4 x 1mg Ask for price

LY 344864

HY-13788 10mM/1mL
EUR 156

LY 3000328

HY-15533 5mg
EUR 365

LY 303511

HY-15643 50mg
EUR 972

LY-411575

HY-50752 100mg
EUR 899

LY-3381916

HY-111540 10mM/1mL
EUR 250

LY-2940094

HY-114452 10mM/1mL
EUR 618

LY-364947

HY-13462 50mg
EUR 461

LY 178002

HY-101579 1mg
EUR 326

LY 345899

HY-101943 10mg
EUR 911

LY 2886721

E1KS2156 5mg
EUR 874

LY-294,002

GL4623-1MG 1 mg
EUR 61

LY-294,002

GL4623-100MG 100 mg
EUR 341

LY-294,002

GL4623-25MG 25 mg
EUR 158

LY-294,002

GL4623-5MG 5 mg
EUR 90

LY 294002

20-abx076741
  • EUR 676.00
  • EUR 286.00
  • 25 mg
  • 5 mg

LY 225910

B6550-10 10 mg
EUR 302

LY 225910

B6550-50 50 mg
EUR 1114

LY 235959

B6551-10 10 mg
EUR 340

LY 235959

B6551-50 50 mg
EUR 1276

LY 367385

B6649-10 10 mg
EUR 340
Description: IC50: 8.8 ?MLY 367385 is a selective mGlu1a receptor antagonist for blockade of quisqualate-induced phosphoinositide hydrolysis.

LY 367385

B6649-50 50 mg
EUR 1276
Description: IC50: 8.8 ?MLY 367385 is a selective mGlu1a receptor antagonist for blockade of quisqualate-induced phosphoinositide hydrolysis.

LY 231617

B6671-10 10 mg
EUR 318

LY 231617

B6671-50 50 mg
EUR 1178

LY 215840

B6776-10 10 mg
EUR 373

LY 215840

B6776-50 50 mg
EUR 1363

LY 255283

B6978-10 10 mg
EUR 208

LY 255283

B6978-25 25 mg
EUR 347

LY 255283

B6978-5 5 mg
EUR 155

LY 320135

B7036-10 10 mg
EUR 276

LY 320135

B7036-5 5 mg
EUR 180

LY 379268

B7061-10 10 mg
EUR 390
Description: LY 379268 is a highly selective group II mGlu receptor agonist with EC50 value of 2.69 and 4.48 nM for hmGlu2 and hmGlu3, respectively [1].

LY 379268

B7061-5 5 mg
EUR 257
Description: LY 379268 is a highly selective group II mGlu receptor agonist with EC50 value of 2.69 and 4.48 nM for hmGlu2 and hmGlu3, respectively [1].

LY 233053

B5124-1 1 mg
EUR 203

LY 233053

B5124-10 10 mg
EUR 366

LY 233053

B5124-50 50 mg
EUR 1347

LY 288513

B5125-10 10 mg
EUR 528

LY 288513

B5125-50 50 mg
EUR 2023

LY 78335

B5521-10 10 mg
EUR 226

LY 78335

B5521-50 50 mg
EUR 795

LY 294002

A8250-10 10 mg
EUR 154
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-5.1 10 mM (in 1mL DMSO)
EUR 113
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-50 50 mg
EUR 293
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 294002

A8250-S Evaluation Sample
EUR 81
Description: LY294002 is a potent inhibitor of class I phosphoinositide 3-kinases (PI3Ks) [1, 2]. It is cell permeable and reversible, and selective against p110?, p110?, p110? and p110?, which acts on ATP binding site of the catalytic subunit.PI3K family is divided into 3 classes: class I, II and III.

LY 354740

B7328-10 10 mg
EUR 231

LY 354740

B7328-5 5 mg
EUR 168

(±)-LY 395756

B7338-10 10 mg
EUR 502

(±)-LY 395756

B7338-50 50 mg
EUR 1958

LY 393558

B7377-10 10 mg
EUR 389

LY 393558

B7377-50 50 mg
EUR 1476

LY 311727

B7447-10 10 mg
EUR 293

LY 311727

B7447-5 5 mg
EUR 180

LY 2087101

B7597-10 10 mg
EUR 350

LY 2087101

B7597-50 50 mg
EUR 1266

LY 303511

A3568-10 10 mg
EUR 321
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 303511

A3568-5 5 mg
EUR 231
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 303511

A3568-50 50 mg
EUR 1262
Description: Description:IC50 Value:N/ALY303511, an inactive analogue of LY294002, is a mTOR inhibitor that did not inhibit PI3-K.in vitro: 100 ?M LY303511 significantly reduced the fraction of cells in S phase.

LY 344864

A3569-10 10 mg
EUR 248
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-5 5 mg
EUR 176
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-5.1 10 mM (in 1mL DMSO)
EUR 189
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY 344864

A3569-50 50 mg
EUR 737
Description: IC50 Value: 6 nM?Ki? LY344864 is a selective receptor agonist with an affinity of 6 nM (Ki) at the recently cloned 5-HT1F receptor. It possesses little affinity for the 56 other serotonergic and non-serotonergic neuronal binding sites examined [1].

LY-411575

A4019-10 10 mg
EUR 200
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-100 100 mg
EUR 711
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-5 5 mg
EUR 134
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-5.1 10 mM (in 1mL DMSO)
EUR 200
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-411575

A4019-50 50 mg
EUR 502
Description: LY-411575 is a potent inhibitor of ?-secretase with IC50 value of 0.078 nM in membrane assay.[1]?-Secertase is one of intramenbrane-cleaving aspartyl protease which cleaves many type-I membrane proteins and many of them have important biological functions.

LY-2835219

B1039-10
EUR 185

LY-2835219

B1039-50
EUR 588

LY-2090314

B1043-25
EUR 544

LY-2090314

B1043-5
EUR 175

LY-83583

B1314-25
EUR 414

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