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-2874455

9532-25
EUR 756

LY-2874455

9532-5
EUR 229

LY-2940680

9604-25
EUR 631

LY-2940680

9604-5
EUR 196

LY-2109761

9605-25
EUR 756

LY-2109761

9605-5
EUR 229

LY-2584702

9445-25
EUR 457

LY-2584702

9445-5
EUR 153

LY-2157299

9475-25
EUR 468

LY-2157299

9475-5
EUR 164

LY-3381916

B2729-25 25 mg
EUR 591

LY-3381916

B2729-5 5 mg
EUR 186

LY-341495

2875-1
EUR 142

LY-341495

2875-5
EUR 414

LY-411575

2648-1
EUR 142

LY-411575

2648-5
EUR 414

LY 294002

1667-25
EUR 387

LY 294002

1667-5
EUR 142

LY 303511

B1734-1
EUR 185

LY 303511

B1734-5
EUR 588

LY-2784544

B1914-25
EUR 588

LY-2784544

B1914-5
EUR 185

LY-2603618

B2191-25
EUR 544

LY-2603618

B2191-5
EUR 175

LY-3200882

B2350-1
EUR 142

LY-3200882

B2350-5
EUR 414

LY-2795050

B2351-25
EUR 631

LY-2795050

B2351-5
EUR 196

LY-2510924

B2360-25
EUR 457

LY-2510924

B2360-5
EUR 153

LY-2090314

B1043-25
EUR 544

LY-2090314

B1043-5
EUR 175

LY-83583

B1314-25
EUR 414

LY-83583

B1314-5
EUR 142

LY 294002

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

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 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 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].

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