Ini1 rabbit pAb

Ini1 rabbit pAb

AO-06-ES8530-50

Ini1 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES8530
Product nameIni1 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameSMARCB1 BAF47 INI1 SNF5L1
Size50μL
Unit price ($)148
Human gene ID6598
Human Swiss-ProtQ12824
SourceRabbit
IsotypeIgG
TargetINI-1
Fields>>Viral life cycle - HIV-1;>>Thermogenesis;>>Hepatocellular carcinoma
Gene nameSMARCB1 BAF47 INI1 SNF5L1
Protein nameSWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID20587
Mouse gene link
Mouse Swiss-ProtQ9Z0H3
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenSynthetic peptide from human protein at AA range: 331-380
SpecificityThe antibody detects endogenous Ini1 protein
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWB 1:500-2000, ELISA 1:10000-20000
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)45kD
BackgroundThe protein encoded by this gene is part of a complex that relieves repressive chromatin structures, allowing the transcriptional machinery to access its targets more effectively. The encoded nuclear protein may also bind to and enhance the DNA joining activity of HIV-1 integrase. This gene has been found to be a tumor suppressor, and mutations in it have been associated with malignant rhabdoid tumors. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Dec 2015],
Functiondisease:Defects in SMARCB1 are a cause of rhabdoid tumor (RDT) [MIM:609322]; also called malignant rhabdoid tumor (MRT). Tumor suppressor. Inactivated in rhabdoid tumors. Rhabdoid tumors are a highly malignant group of neoplasms that usually occur in early childhood. SMARCB1/INI1 is also frequently inactivated in epithelioid sarcomas.,disease:Defects in SMARCB1 are a cause of schwannomatosis [MIM:162091]; also called congenital cutaneous neurilemmomatosis. Schwannomas are benign tumors of the peripheral nerve sheath that usually occur singly in otherwise normal individuals. Multiple schwannomas in the same individual suggest an underlying tumor-predisposition syndrome. The most common such syndrome is NF2. The hallmark of NF2 is the development of bilateral vestibular-nerve schwannomas; but two-thirds or more of all NF2-affected individuals develop schwannomas in other locations, and der
Subcellular locationNucleus.
ExpressionBra

Additional Images

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Western Blot analysis of HEPG2 cells using Antibody diluted at 800. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
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: AO-06-ES8530-50
: 10 Produits
Hurry! only 10 items left in stock.

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