Anti-Ki67 Antibody Picoband™ (monoclonal, 5C7) | Boster M00254-9 product information

This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.

product summary

company name :

Boster

product type :

antibody

product name :

Anti-Ki67 Antibody Picoband™ (monoclonal, 5C7)

catalog :

M00254-9

quantity :

100 µg/vial

clonality :

monoclonal

host :

mouse

conjugate :

nonconjugated

clone name :

5C7

reactivity :

human

application :

western blot, immunocytochemistry, flow cytometry, immunohistochemistry - paraffin section

product information

SKU :

M00254-9

Product Name :

Anti-Ki67 Antibody Picoband™ (monoclonal, 5C7)

Size :

100 µg/vial

Clonality :

Monoclonal

Clone Number :

5C7

Host :

Mouse

Reactivity :

Human, Mouse

Application(s) :

WB, IHC-P, ICC, IF, Flow Cytometry

Application Details :

Western blot, 0.25-0.5 µg/ml, Human, Mouse. Immunohistochemistry(Paraffin-embedded Section), 2-5 µg/ml, Human. Immunocytochemistry/Immunofluorescence, 5 µg/ml, Human. Flow Cytometry, 1-3 µg/1x10^6 cells, Human.

Description :

Boster Bio Anti-Ki67 Antibody Picoband™ (monoclonal, 5C7) catalog # M00254-9. Tested in Flow Cytometry, IF, IHC-P, ICC, WB applications. This antibody reacts with Human, Mouse.

Concentration :

Adding 0.2 ml of distilled water will yield a concentration of 500 µg/ml.

Gene Name :

MKI67

Uniprot ID :

P46013

Immunogen :

E. coli-derived human Ki67 recombinant protein (Position: K2860-I3256).

Form :

Lyophilized

Contents :

Each vial contains 4 mg Trehalose, 0.9 mg NaCl and 0.2 mg Na2HPO4.

Purification :

Immunogen affinity purified.

Isotype :

IgG2b

Storage :

At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.

Reconstitution :

Adding 0.2 ml of distilled water will yield a concentration of 500 µg/ml.

Molecular Weight :

24031

Background :

Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease.