89-014-361

JAR (human choriocarcinoma) Whole cell lysate, Non-denatured, Abnova

Manufacturer: Abnova Corporation

Select a Size

Pack Size SKU Availability Price
Each of 1 89-014-361-Each-of-1 In Stock ₹ 22,844.52

89-014-361 - Each of 1

₹ 22,844.52

In Stock

Quantity

1

Base Price: ₹ 22,844.52

GST (18%): ₹ 4,112.014

Total Price: ₹ 26,956.534

For Use With (Application)

Immunoprecipitation, Western Blot

Description

Whole cell lysate (non-denatured)

Preparation Method

Cell lysate was prepared by homogenization in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined with Bradford assay (Bio-Rad protein assay, Microplate Standard assay).

Quantity

200 μg

Host Species

Human

Content And Storage

Store at -80°C. Aliquot to avoid repeated freezing and thawing.

Tissue

Placenta

Lysis Buffer

Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

Quality Control Testing

12.5% SDS-PAGE Stained with Coomassie Blue.

Storage Buffer

In modified RIPA Lysis Buffer.

Concentration

5 mg/mL

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Description

  • Tissue: Placenta Host: Human Lysis Buffer: Modified RIPA Lysis Buffer: 50mM Tris-HCl pH 7.4, 150mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF Storage buffer: In modified RIPA Lysis Buffer Western Blotting, Immunoprecipitation

Compare Similar Items

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Abnova Corporation

89-014-361

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For Use With (Application):
Immunoprecipitation, Western Blot

Description:
Whole cell lysate (non-denatured)

Preparation Method:
Cell lysate was prepared by homogenization in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined with Bradford assay (Bio-Rad protein assay, Microplate Standard assay).

Quantity:
200 μg

Host Species:
Human

Content And Storage:
Store at -80°C. Aliquot to avoid repeated freezing and thawing.

Tissue:
Placenta

Lysis Buffer:
Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

Quality Control Testing:
12.5% SDS-PAGE Stained with Coomassie Blue.

Storage Buffer:
In modified RIPA Lysis Buffer.

Concentration:
5 mg/mL

Img

Abnova Corporation

89-014-362

--


For Use With (Application):
Immunoprecipitation, Western Blot

Description:
Whole cell lysate (non-denatured)

Preparation Method:
Cell lysate was prepared by homogenization in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined with Bradford assay (Bio-Rad protein assay, Microplate Standard assay).

Quantity:
200 μg

Host Species:
Human

Content And Storage:
Store at -80°C. Aliquot to avoid repeated freezing and thawing.

Tissue:
Prostate

Lysis Buffer:
Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

Quality Control Testing:
12.5% SDS-PAGE Stained with Coomassie Blue.

Storage Buffer:
In modified RIPA Lysis Buffer.

Concentration:
5 mg/mL

Img

Abnova Corporation

89-014-363

--


For Use With (Application):
Immunoprecipitation, Western Blot

Description:
Whole cell lysate (non-denatured)

Preparation Method:
Cell lysate was prepared by homogenization in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined with Bradford assay (Bio-Rad protein assay, Microplate Standard assay).

Quantity:
200 μg

Host Species:
Human

Content And Storage:
Store at -80°C. Aliquot to avoid repeated freezing and thawing.

Tissue:
Adrenal Gland (Cortex)

Lysis Buffer:
Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

Quality Control Testing:
12.5% SDS-PAGE Stained with Coomassie Blue.

Storage Buffer:
In modified RIPA Lysis Buffer.

Concentration:
5 mg/mL

Img

Abnova Corporation

89-014-364

--


For Use With (Application):
Immunoprecipitation, Western Blot

Description:
Whole cell lysate (non-denatured)

Preparation Method:
Cell lysate was prepared by homogenization in ice-cold modified RIPA Lysis Buffer with cocktail of protease inhibitors (Sigma). Cell debris was removed by centrifugation. Protein concentration was determined with Bradford assay (Bio-Rad protein assay, Microplate Standard assay).

Quantity:
200 μg

Host Species:
Human

Content And Storage:
Store at -80°C. Aliquot to avoid repeated freezing and thawing.

Tissue:
Breast Duct

Lysis Buffer:
Modified RIPA Lysis Buffer: 50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1mM EDTA, 1% Triton X-100, 0.1% SDS, 1% Sodium deoxycholate, 1mM PMSF.

Quality Control Testing:
12.5% SDS-PAGE Stained with Coomassie Blue.

Storage Buffer:
In modified RIPA Lysis Buffer.

Concentration:
5 mg/mL