FAM65B antibody (AA 1-210)

Catalog No. ABIN6140465

Product Details anti-FAM65B Antibody

Target: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Binding Specificity: AA 1-210

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This FAM65B antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (IF)

Sequence: MLVGSQSFSP GGPNGIIRSQ SFAGFSGLQE RRSRCNSFIE NSSALKKPQA KLKKMHNLGH KNNNPPKEPQ PKRVEEVYRA LKNGLDEYLE VHQTELDKLT AQLKDMKRNS RLGVLYDLDK QIKTIERYMR RLEFHISKVD ELYEAYCIQR RLQDGASKMK QAFATSPASK AARESLTEIN RSFKEYTENM CTIEVELENL LGEFSIKMKG

Cross-Reactivity: Human, Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-210 of human FAM65B (NP_056948.2).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000,IF,1:50 - 1:200

Comment:

HIGH QUALITY

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for FAM65B

Target: FAM65B (Family with Sequence Similarity 65, Member B (FAM65B))

Alternative Name: FAM65B (FAM65B Products)

Synonyms: C6orf32 antibody, DIFF40 antibody, DIFF48 antibody, MYONAP antibody, PL48 antibody, 1700108N18Rik antibody, 6330500D04Rik antibody, AI225904 antibody, E430013J17Rik antibody, si:dkey-218n20.1 antibody, Ab2-162 antibody, RGD1306939 antibody, RHO family interacting cell polarization regulator 2 antibody, family with sequence similarity 65, member B antibody, ripor2 antibody, RIPOR2 antibody, Ripor2 antibody, FAM65B antibody

Background: This gene encodes an atypical inhibitor of the small G protein RhoA. Inhibition of RhoA activity by the encoded protein mediates myoblast fusion and polarization of T cells and neutrophils. The encoded protein is a component of hair cell stereocilia that is essential for hearing. A splice site mutation in this gene results in hearing loss in human patients.,RIPOR2,C6orf32,DFNB104,DIFF40,DIFF48,FAM65B,MYONAP,PL48,Stem Cells,Mesenchymal Stem Cells,FAM65B

Molecular Weight: 65 kDa/118 kDa

Gene ID: 9750

UniProt: Q9Y4F9

Pathways: Transition Metal Ion Homeostasis