SLC4A11 antibody (AA 1-180)

Catalog No. ABIN7270461

Product Details anti-SLC4A11 Antibody

Target: SLC4A11 (Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))

Binding Specificity: AA 1-180

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SLC4A11 antibody is un-conjugated

Application: Western Blotting (WB)

Purpose: SLC4A11 Rabbit pAb

Sequence: MSQVGGRGDR CTQEVQGLVH GAGDLSASLA ENSPTMSQNG YFEDSSYYKC DTDDTFEARE EILGDEAFDT ANSSIVSGES IRFFVNVNLE MQATNTENEA TSGGCVLLHT SRKYLKLKNF KEEIRAHRDL DGFLAQASIV LNETATSLDN VLRTMLRRFA RDPDNNEPNC NLDLLMAMLF

Cross-Reactivity: Human, Mouse

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human SLC4A11 (NP_114423.1).

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

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 SLC4A11

Target: SLC4A11 (Solute Carrier Family 4, Sodium Borate Transporter, Member 11 (SLC4A11))

Alternative Name: SLC4A11 (SLC4A11 Products)

Synonyms: NaBC1 antibody, si:dkey-12j14.4 antibody, AI503023 antibody, BTR1 antibody, CDPD1 antibody, CHED2 antibody, NABC1 antibody, dJ794I6.2 antibody, solute carrier family 4 member 11 antibody, solute carrier family 4 member 11 L homeolog antibody, solute carrier family 4, sodium borate transporter, member 11 antibody, solute carrier family 4, sodium bicarbonate transporter-like, member 11 antibody, Slc4a11 antibody, SLC4A11 antibody, slc4a11.L antibody, slc4a11 antibody

Background: This gene encodes a voltage-regulated, electrogenic sodium-coupled borate cotransporter that is essential for borate homeostasis, cell growth and cell proliferation. Mutations in this gene have been associated with a number of endothelial corneal dystrophies including recessive corneal endothelial dystrophy 2, corneal dystrophy and perceptive deafness, and Fuchs endothelial corneal dystrophy. Multiple transcript variants encoding different isoforms have been described.,SLC4A11,BTR1,CDPD1,CHED,CHED2,NABC1,dJ794I6.2,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,SLC4A11

Molecular Weight: 45kDa/98kDa/99kDa/103kDa

Gene ID: 83959

UniProt: Q8NBS3

Pathways: Proton Transport