MNX1/HB9/HLXB9 Polyclonal Antibody

Dodavatel:

Reddot Biotech USA Inc.

Teplota skladování:

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

Katalogové číslo:

RD89321A/60

60μL

7 728,00 Kč

NA OBJEDNÁNÍ

RD89321A/120

120μL

12 365,00 Kč

NA OBJEDNÁNÍ

RD89321A/200

200μL

20 479,00 Kč

NA OBJEDNÁNÍ

Velikost balení:

Cena bez DPH:

Dostupnost:

Vložit do košíku

Zobrazovat ceny: bez DPH / včetně DPH

This is a MNX1/HB9/HLXB9 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

This gene encodes a nuclear protein, which contains a homeobox domain and is a transcription factor. Mutations in this gene result in Currarino syndrome, an autosomic dominant congenital malformation. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2009]

Technická specifikace

Clonality		Polyclonal
Purification Method		Affinity purification
Isotype		IgG
Host		Rabbit
Immunogen		Recombinant fusion protein of human MNX1/HB9/HLXB9
Gene ID		3110
Swissprot		P50219
Calculated MW		32kDa
Observed MW		34-38KDa
Reactivity		Human,Mouse,Rat
Applications		WB
Conjugation		Unconjugated
Dilution		WB 1:500-1:2000
Concentration		1mg/mL
Buffer		PBS with 0.05% proclin300,50% glycerol,pH7.3.

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MNX1/HB9/HLXB9 Polyclonal Antibody

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